Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

Base Information

Chemical Name:Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester
CAS No.:210104-39-5
Molecular Formula:C₂₅H₃₄O₇S
Molecular Weight:478.607
Hs Code.:

Synonyms:Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

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Chemical Property of Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

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Technology Process of Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

There total 3 articles about Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester 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: 96.0%

: 63584-47-4
(1-tert-butylsulfanyl-vinyloxy)trimethylsilane

: 210104-29-3
Acetic acid 2-[(2S,4S,5R)-5-(2-acetoxy-ethyl)-2-phenylethynyl-[1,3]dioxolan-4-yl]-ethyl ester

: 210104-39-5
Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

Guidance literature:: With B-phenyl-oxazaborolidine derivative; In dichloromethane; at -78 ℃; for 15h;
DOI:10.1016/S0040-4039(98)00823-5

Reference yield:

: 6142-95-6
phenylpropargyl aldehyde diethyl acetal

: 210104-39-5
Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 31 percent / p-TsOH, molecular sieves 4A / CH₂Cl₂ / Ambient temperature

2: 96 percent / B-phenyl-oxazaborolidine derivative / CH₂Cl₂ / 15 h / -78 °C

With 4 A molecular sieve; B-phenyl-oxazaborolidine derivative; toluene-4-sulfonic acid; In dichloromethane;
DOI:10.1016/S0040-4039(98)00823-5

Reference yield:

: Acetic acid (3R,4S)-6-acetoxy-3,4-dihydroxy-hexyl ester

: 210104-39-5
Acetic acid (3R,4S)-6-acetoxy-3-((S)-1-tert-butylsulfanylcarbonylmethyl-3-phenyl-prop-2-ynyloxy)-4-hydroxy-hexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 31 percent / p-TsOH, molecular sieves 4A / CH₂Cl₂ / Ambient temperature

2: 96 percent / B-phenyl-oxazaborolidine derivative / CH₂Cl₂ / 15 h / -78 °C

With 4 A molecular sieve; B-phenyl-oxazaborolidine derivative; toluene-4-sulfonic acid; In dichloromethane;
DOI:10.1016/S0040-4039(98)00823-5