(4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

Base Information

Chemical Name:(4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone
CAS No.:76596-39-9
Molecular Formula:C₁₀H₁₆O₄S
Molecular Weight:232.301
Hs Code.:

Synonyms:(4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

Suppliers and Price of (4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

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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 (4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

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Technology Process of (4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

There total 5 articles about (4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone 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: 40.0%

: 107-03-9
1-thiopropane

: 5831-38-9,24292-29-3,25163-24-0,39910-94-6,62929-65-1,67772-76-3,439906-13-5
(+/-)-Epiepoxydon

: 76596-39-9
(4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

Guidance literature:: In acetic acid; at 70 ℃; for 1h;
DOI:10.1021/ja00547a052

Reference yield:

: (1S,2S,3R,4R,5R,6S)-3-Bromo-4-hydroxymethyl-5-trimethylsilanyl-7-oxa-bicyclo[4.1.0]heptan-2-ol

: 76596-39-9
(4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / pyridine / CH₂Cl₂ / -20 °C

2: 98 percent / Jones reagent

3: 68 percent / NaHCO₃ / methanol

4: 40 percent / acetic acid / 1 h / 70 °C

With pyridine; jones reagent; sodium hydrogencarbonate; In methanol; dichloromethane; acetic acid;
DOI:10.1021/ja00547a052

Reference yield:

: 76596-32-2
(1S,2R,4S,5R,6S,9R)-9-Bromo-5-trimethylsilanyloxy-3,8-dioxa-tricyclo[4.2.1.0^2,4]nonan-7-one

: 76596-39-9
(4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / lithium borohydride / tetrahydrofuran / 21 h / Ambient temperature

2: 95 percent / pyridine / CH₂Cl₂ / -20 °C

3: 98 percent / Jones reagent

4: 68 percent / NaHCO₃ / methanol

5: 40 percent / acetic acid / 1 h / 70 °C

With pyridine; lithium borohydride; jones reagent; sodium hydrogencarbonate; In tetrahydrofuran; methanol; dichloromethane; acetic acid;
DOI:10.1021/ja00547a052