(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

Base Information

Chemical Name:(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester
CAS No.:95531-85-4
Molecular Formula:C₃₃H₅₄O₅Si
Molecular Weight:558.874
Hs Code.:

(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

Synonyms:(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

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Chemical Property of (1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

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Technology Process of (1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

There total 9 articles about (1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic 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:

: 95532-02-8
(4R,4aR,8aS)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-4a-methyl-octahydro-naphthalen-2-one

: 95531-85-4
(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) sodium herxamethyldisilazide / tetrahydrofuran / 1.) 0 degC, 7 h; 2.) -78 degC, 1 h

2: 89 percent / potassium tert-butoxide, sodium iodide / hexamethylphosphoric acid triamide / 6 h / 60 °C

3: 86 percent / nonane / 36 h / Heating

4: LiAlH₄ / 0.5 h / 0 °C

With lithium aluminium tetrahydride; potassium tert-butylate; sodium hexamethyldisilazane; sodium iodide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; nonane;
DOI:10.1021/ja00295a027

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 95531-85-4
(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 91 percent / triethylamine, 4-dimethylaminopyridine / CH₂Cl₂ / 4 h / 25 °C

2: 1.) sodium herxamethyldisilazide / tetrahydrofuran / 1.) 0 degC, 7 h; 2.) -78 degC, 1 h

3: 89 percent / potassium tert-butoxide, sodium iodide / hexamethylphosphoric acid triamide / 6 h / 60 °C

4: 86 percent / nonane / 36 h / Heating

5: LiAlH₄ / 0.5 h / 0 °C

With dmap; lithium aluminium tetrahydride; potassium tert-butylate; sodium hexamethyldisilazane; triethylamine; sodium iodide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; nonane; dichloromethane;
DOI:10.1021/ja00295a027

Reference yield:

: 95531-79-6
(1R,2R,4aS,8aR)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-8a-methyl-3-oxo-decahydro-naphthalene-2-carboxylic acid methyl ester

: 95531-85-4
(1S,2S,3S,4aS,8aR)-2-[(R)-1-(2-Benzyloxy-ethyl)-2-methyl-allyl]-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-8a-methyl-decahydro-naphthalene-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / potassium tert-butoxide, sodium iodide / hexamethylphosphoric acid triamide / 6 h / 60 °C

2: 86 percent / nonane / 36 h / Heating

3: LiAlH₄ / 0.5 h / 0 °C

With lithium aluminium tetrahydride; potassium tert-butylate; sodium iodide; In N,N,N,N,N,N-hexamethylphosphoric triamide; nonane;
DOI:10.1021/ja00295a027