(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

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Chemical Name:(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester
CAS No.:173092-01-8
Molecular Formula:C₃₂H₄₉NO₄Si
Molecular Weight:539.831
Hs Code.:

(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

Synonyms:(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

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Chemical Property of (S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

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Technology Process of (S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

There total 8 articles about (S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl 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:

: 136159-65-4,96930-27-7
(S)-4-benzyl-3-(3-phenylpropanoyl)oxazolidin-2-one

: 173092-01-8
(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) NaHMDS / 1.) THF, -78 deg C, 15 min, 2.) THF, from -78 deg C to 0 deg C, 60 min

2: 1.) n-BuLi / 1.) hexane, THF, 0 deg C, 2.) hexane, THF, 0 deg C, 15 min

3: LAH / tetrahydrofuran / 0.5 h / 0 °C

4: 97 percent / imidazole / dimethylformamide / Ambient temperature

5: 1.) O₃, 2.) Ph₃P / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, RT, overnight

6: CHCl₃; toluene / 4 h

7: KHMDS / 1.) THF, toluene, 20 min, 2.) THF, toluene, 0 deg C, 25 min

With 1H-imidazole; lithium aluminium tetrahydride; n-butyllithium; sodium hexamethyldisilazane; potassium hexamethylsilazane; ozone; triphenylphosphine; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; toluene;
DOI:10.1021/ja00150a011

Reference yield:

: 173091-87-7
(R)-3-Benzyl-4-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde

: 173092-01-8
(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: CHCl₃; toluene / 4 h

2: KHMDS / 1.) THF, toluene, 20 min, 2.) THF, toluene, 0 deg C, 25 min

With potassium hexamethylsilazane; In chloroform; toluene;
DOI:10.1021/ja00150a011

Reference yield:

: 173092-00-7
(S)-2-benzyl-5-methyl-hex-4-en-1-ol

: 173092-01-8
(S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-phenyl-ethyl]-2-isobutyl-2-(3-methyl-but-2-enyl)-3-oxo-2,3-dihydro-pyrrole-1-carboxylic acid allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / imidazole / dimethylformamide / Ambient temperature

2: 1.) O₃, 2.) Ph₃P / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, RT, overnight

3: CHCl₃; toluene / 4 h

4: KHMDS / 1.) THF, toluene, 20 min, 2.) THF, toluene, 0 deg C, 25 min

With 1H-imidazole; potassium hexamethylsilazane; ozone; triphenylphosphine; In chloroform; N,N-dimethyl-formamide; toluene;
DOI:10.1021/ja00150a011