Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

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Chemical Name:Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester
CAS No.:250139-14-1
Molecular Formula:C₂₅H₃₈O₅S
Molecular Weight:450.64
Hs Code.:

Synonyms:Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

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Chemical Property of Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

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Technology Process of Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

There total 6 articles about Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl 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: 69.0%

: 37577-72-3
2,3-dimethylhydroquinone monoacetate

: 116119-14-3
Acetic acid (R)-1-(2-isopropylsulfanyl-ethyl)-1,5-dimethyl-hex-4-enyl ester

: 250139-14-1
Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

: Acetic acid 5-[1-((R)-3-acetoxy-3,7-dimethyl-oct-6-enylsulfanyl)-1-methyl-ethyl]-4-hydroxy-2,3-dimethyl-phenyl ester

Guidance literature:: With sulfuryl dichloride; triethylamine; In dichloromethane; at -78 - 25 ℃;
DOI:10.1016/S0040-4039(99)01204-6

Reference yield:

: 106-24-1
Geraniol

: 250139-14-1
Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: D-(-)-DET; tert-BuOOH; Ti(i-PrO)4 / -25 °C

2: 99 percent / LiALH₄ / -40 - 25 °C

3: pyridine / -10 °C

4: tetrahydrofuran

5: DMAP; NEt₃ / CH₂Cl₂

6: 69 percent / sulfuryl chloride; NEt₃ / CH₂Cl₂ / -78 - 25 °C

With pyridine; titanium(IV) isopropylate; tert.-butylhydroperoxide; dmap; lithium aluminium tetrahydride; sulfuryl dichloride; diethyl (2S,3S)-tartrate; triethylamine; In tetrahydrofuran; dichloromethane; 1: Sharpless asymmetric epoxidation / 2: Reduction / 3: Tosylation / 4: Substitution / 5: Acetylation / 6: Substitution;
DOI:10.1016/S0040-4039(99)01204-6

Reference yield:

: 50727-94-1,62777-72-4,62960-04-7,71030-55-2,76985-26-7,82188-73-6,112456-40-3,112456-65-2,62777-71-3
(2R,3R)-3-methyl-3-(4-methyl-3-pentenyl)oxiranemethanol

: 250139-14-1
Acetic acid 5-((R)-3-acetoxy-1-isopropylsulfanyl-3,7-dimethyl-oct-6-enyl)-4-hydroxy-2,3-dimethyl-phenyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / LiALH₄ / -40 - 25 °C

2: pyridine / -10 °C

3: tetrahydrofuran

4: DMAP; NEt₃ / CH₂Cl₂

5: 69 percent / sulfuryl chloride; NEt₃ / CH₂Cl₂ / -78 - 25 °C

With pyridine; dmap; lithium aluminium tetrahydride; sulfuryl dichloride; triethylamine; In tetrahydrofuran; dichloromethane; 1: Reduction / 2: Tosylation / 3: Substitution / 4: Acetylation / 5: Substitution;
DOI:10.1016/S0040-4039(99)01204-6