Comments on: LiAlH[Ot-Bu]3 For The Reduction of Acid Halides To Aldehydes https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/ Tue, 23 Apr 2024 16:21:38 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: James Ashenhurst https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-691742 Tue, 23 Apr 2024 16:21:35 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-691742 In reply to Dániel Budai.

Fixed – thank you!

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By: Dániel Budai https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-691687 Tue, 23 Apr 2024 06:48:42 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-691687 Hi James, there’s a typo in the beginning of the article:

“Acid halides can also be reduced to acid halides using Pd-C / barium carbonate with hydrogen, otherwise known as Rosenmund’s catalyst”

I assume the second “acid halides” should be “aldehydes” :)

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By: chandru https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-686293 Fri, 01 Mar 2024 01:16:11 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-686293 hey james what is the neccesity to install such bulky groups ?

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By: Cuando el ácido 2,3-dimetilhexanoico se trata con SOCl2 / piridina, seguido de LiAl [OC (CH3) 3] 3H, ¿cuál sería el producto? Gracias – ElbuhoSabio https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-585550 Thu, 01 Oct 2020 17:08:59 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-585550 […] el gran compuesto de aluminio (tri-litiotert-butoxialuminio hidruroCh. 20 Química Orgánica, Paula Yurkanis Bruice) con los grupos donadores de electrones permite que […]

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By: Quando l’acido 2,3-dimetilesanoico viene trattato con SOCl2 / piridina, seguito da LiAl [OC (CH3) 3] 3H, quale sarebbe il prodotto ???? Grazie – GufoSaggio https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-573876 Fri, 27 Dec 2019 11:38:30 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-573876 […] il grande composto di alluminio (litio tri-terz-idruro di alluminio e butossialuminio, Cap. 20, Chimica organica, Paula Yurkanis Bruice) con i gruppi donatori di elettroni consente al […]

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By: James Ashenhurst https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-568887 Sat, 26 Oct 2019 01:03:12 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-568887 In reply to Dakota.

It will deprotonate them but not add, that’s about it.

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By: Dakota https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-568826 Thu, 24 Oct 2019 20:46:17 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-568826 Does LTBA react with carboxylic acids?

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By: Chris G. https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-529907 Sun, 25 Mar 2018 22:50:29 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-529907 What happens if you add LAH to an acyl chloride? Would the acyl chloride reduce to an alcohol or would no reaction occur?

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By: Michael https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-510520 Wed, 05 Apr 2017 00:55:08 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-510520 Would it be possible to use DIBAL-H instead of Li(O-t-Bu)3?

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By: James https://www.masterorganicchemistry.com/2011/11/11/reagent-friday-lialhocch333/#comment-359965 Mon, 02 Feb 2015 22:17:20 +0000 https://www.masterorganicchemistry.com/?p=2819#comment-359965 In reply to ben.

Yes! On a personal note I have tried both the in situ prep and buying it from Aldrich and had better luck with the store-bought reagent.

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