(S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol

Base Information

Chemical Name:(S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol
CAS No.:266694-65-9
Molecular Formula:C₂₀H₃₀O₃S
Molecular Weight:350.522
Hs Code.:

Synonyms:(S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol

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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)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol

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Technology Process of (S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol

There total 2 articles about (S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol 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: 87.0%

: 266694-61-5
(S)-3-Hydroxy-3-phenyl-3-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propionic acid tert-butyl ester

: 266694-65-9
(S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 2h; Heating;
DOI:10.1002/jccs.200000006

Reference yield:

: 266694-57-9
Phenyl-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-methanone

: 266694-65-9
(S)-1-Phenyl-1-((2R,4aR,7R,8aR)-4,4,7-trimethyl-hexahydro-1-oxa-3-thia-naphthalen-2-yl)-propane-1,3-diol

Guidance literature:: Multi-step reaction with 2 steps

1.1: Mg; I; MgCl₂ / tetrahydrofuran

1.2: tetrahydrofuran / 4 h / 32 °C

2.1: 87 percent / LiAlH₄ / diethyl ether / 2 h / Heating

With lithium aluminium tetrahydride; magnesium; magnesium chloride; In tetrahydrofuran; diethyl ether; 1.1: enolization / 1.2: Alkylation / 2.1: Reduction;
DOI:10.1002/jccs.200000006