(S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

Base Information

Chemical Name:(S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one
CAS No.:1373432-30-4
Molecular Formula:C₁₈H₂₃NO₂S₂
Molecular Weight:349.518
Hs Code.:

Synonyms:(S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

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Technology Process of (S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

There total 1 articles about (S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%

: 924265-91-8
(S)-1-(4-mesityl-2-thioxothiazolidin-3-yl)ethanone

: 7319-38-2
3-butenal

: 1373432-30-4
(S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

Guidance literature:: (S)-1-(4-mesityl-2-thioxothiazolidin-3-yl)ethanone; With titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at -78 - 0 ℃;

3-butenal; In dichloromethane; at -78 ℃; for 1h; optical yield given as %de;
DOI:10.1021/ol300785c

Reference yield: 96.0%

: 1373432-30-4
(S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

: 79271-56-0
triethylsilyl trifluoromethyl sulfonate

: 1373432-45-1
(S)-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)-3-(triethylsilyloxy)hex-5-en-1-one

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/ol300785c

Reference yield:

: 1373432-30-4
(S)-3-hydroxy-1-((S)-4-mesityl-2-thioxothiazolidin-3-yl)hex-5-en-1-one

: 1373432-46-2
(5S,10R,14S,15R,17S,18S,E)-5-allyl-10-(tert-butyldimethylsilyloxy)-3,3-diethyl-7-hydroxy-20,20-diisopropyl-15-(4-methoxybenzyloxy)-10,14,17,18,21-pentamethyl-4,19-dioxa-3,20-disiladocos-11-en-9-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: 2,6-dimethylpyridine / dichloromethane / 0 - 20 °C

2.1: diisobutylaluminium hydride / hexane; dichloromethane / -78 °C

3.1: lithium diisopropyl amide / tetrahydrofuran / 3 h / -78 °C

3.2: 3 h / -78 °C

With 2,6-dimethylpyridine; diisobutylaluminium hydride; lithium diisopropyl amide; In tetrahydrofuran; hexane; dichloromethane; 3.1: Aldol condensation / 3.2: Aldol condensation;
DOI:10.1021/ol300785c