3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

Base Information

Chemical Name:3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester
CAS No.:462628-23-5
Molecular Formula:C₂₉H₄₀O₃Si
Molecular Weight:464.72
Hs Code.:

Synonyms:3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

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Chemical Property of 3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

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Technology Process of 3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

There total 4 articles about 3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic 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: 98.0%

: 462628-21-3
3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentane carbaldehyde

: 462628-23-5
3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

Guidance literature:: Methyl diethylphosphonoacetate; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.75h;

3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentane carbaldehyde; In tetrahydrofuran; at 0 ℃; for 3.33333h;

Reference yield: 98.0%

: 1067-74-9
Methyl diethylphosphonoacetate

: 462628-21-3
3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentane carbaldehyde

: 462628-23-5
3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1016/S0960-894X(02)00221-4

Reference yield:

: 560-09-8
(1S,3R)-(-)-camphoric acid

: 462628-23-5
3-[3-(tert-butyl-diphenyl-silanyloxymethyl)-1,2,2-trimethyl-cyclopentyl]-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / LiAlH₄ / tetrahydrofuran; diethyl ether / 5 h / 20 °C

2: 86 percent / imidazole / dimethylformamide / 5 h / 0 - 20 °C

3: 97 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 0 °C

4: 98 percent / NaH / tetrahydrofuran / 2 h / 0 °C

With 1H-imidazole; lithium aluminium tetrahydride; oxalyl dichloride; sodium hydride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; 3: Swern oxidation / 4: Horner-Emmons reaction;
DOI:10.1016/S0960-894X(02)00221-4