(4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

Base Information

Chemical Name:(4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester
CAS No.:410072-04-7
Molecular Formula:C₂₇H₄₀O₅Si
Molecular Weight:472.697
Hs Code.:

Synonyms:(4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

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Chemical Property of (4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

Chemical Property:

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Technology Process of (4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

There total 7 articles about (4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl 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:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 410072-04-7
(4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 91.5 percent / imidazole / dimethylformamide / 1 h / 20 °C

2: DIBAL / CH₂Cl₂; toluene / 0.33 h / -78 °C

3: H₂NOH*HCl; NaOAc / ethanol / 1 h / 20 °C

4: 20.0 g / aq. NaClO / CH₂Cl₂ / 3.5 h / 20 °C

5: 66.4 percent / Zn; AcOH / 4 h / 20 °C

6: mCPBA; AcOH / 41 h / 20 °C

7: 9.49 g / K₂CO₃ / 0.75 h / 20 °C

With 1H-imidazole; sodium hypochlorite; hydroxylamine hydrochloride; sodium acetate; diisobutylaluminium hydride; potassium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; zinc; In ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; 6: Baeyer-Villiger oxidation;
DOI:10.1021/ja0177049

Reference yield:

: 4-(tert-butyl-diphenyl-silanyloxymethyl)-6-ethyl-hept-6-enal

: 410072-04-7
(4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: H₂NOH*HCl; NaOAc / ethanol / 1 h / 20 °C

2: 20.0 g / aq. NaClO / CH₂Cl₂ / 3.5 h / 20 °C

3: 66.4 percent / Zn; AcOH / 4 h / 20 °C

4: mCPBA; AcOH / 41 h / 20 °C

5: 9.49 g / K₂CO₃ / 0.75 h / 20 °C

With sodium hypochlorite; hydroxylamine hydrochloride; sodium acetate; potassium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; zinc; In ethanol; dichloromethane; 4: Baeyer-Villiger oxidation;
DOI:10.1021/ja0177049

Reference yield:

: 410071-88-4
(4R)-4-(tert-butyldiphenylsilyloxymethyl)-6-ethylhept-6-enenitrile

: 410072-04-7
(4R,6S)-4-(tert-butyldiphenylsilyloxymethyl)-6-hydroxy-6-(hydroxymethyl)octanoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: DIBAL / CH₂Cl₂; toluene / 0.33 h / -78 °C

2: H₂NOH*HCl; NaOAc / ethanol / 1 h / 20 °C

3: 20.0 g / aq. NaClO / CH₂Cl₂ / 3.5 h / 20 °C

4: 66.4 percent / Zn; AcOH / 4 h / 20 °C

5: mCPBA; AcOH / 41 h / 20 °C

6: 9.49 g / K₂CO₃ / 0.75 h / 20 °C

With sodium hypochlorite; hydroxylamine hydrochloride; sodium acetate; diisobutylaluminium hydride; potassium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; zinc; In ethanol; dichloromethane; toluene; 5: Baeyer-Villiger oxidation;
DOI:10.1021/ja0177049