(4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

Base Information

Chemical Name:(4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester
CAS No.:392724-95-7
Molecular Formula:C₃₁H₅₃NO₆Si
Molecular Weight:563.85
Hs Code.:

(4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

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Chemical Property of (4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

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Technology Process of (4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

There total 13 articles about (4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl 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:

: 20160-60-5
2-(trimethylsilyl)-ethoxycarbonyl chloride

: 392724-95-7
(4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 59 percent / tetrahydrofuran / -50 - 20 °C

2.1: 90 percent / Grubbs catalyst / CH₂Cl₂ / 24 h / Heating

3.1: 84 percent / m-CPBA / CH₂Cl₂ / 12 h / 0 °C

4.1: chiral Jacobsen (S,S)-Cr(salen) catalyst / 120 h / 20 °C

4.2: NaH / dimethylformamide / 1 h / 20 °C

4.3: 1.11 mg / TBAI / dimethylformamide / 12 h / 20 °C

With chiral Jacobsen (S,S)-Cr(salen) catalyst; 3-chloro-benzenecarboperoxoic acid; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(03)00857-3

Reference yield:

: 132365-02-7
N-benzyl-N-(but-3-enyl)-but-3-en-1-amine

: 392724-95-7
(4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 59 percent / tetrahydrofuran / -50 - 20 °C

2.1: 90 percent / Grubbs catalyst / CH₂Cl₂ / 24 h / Heating

3.1: 84 percent / m-CPBA / CH₂Cl₂ / 12 h / 0 °C

4.1: chiral Jacobsen (S,S)-Cr(salen) catalyst / 120 h / 20 °C

4.2: NaH / dimethylformamide / 1 h / 20 °C

4.3: 1.11 mg / TBAI / dimethylformamide / 12 h / 20 °C

With chiral Jacobsen (S,S)-Cr(salen) catalyst; 3-chloro-benzenecarboperoxoic acid; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(03)00857-3

Reference yield:

: 392724-87-7
di-but-3-enyl-carbamic acid 2-trimethylsilanyl-ethyl ester

: 392724-95-7
(4R,5R)-4-[(S)-3-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-butoxy]-5-isobutoxy-azepane-1-carboxylic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 90 percent / Grubbs catalyst / CH₂Cl₂ / 24 h / Heating

2.1: 84 percent / m-CPBA / CH₂Cl₂ / 12 h / 0 °C

3.1: chiral Jacobsen (S,S)-Cr(salen) catalyst / 120 h / 20 °C

3.2: NaH / dimethylformamide / 1 h / 20 °C

3.3: 1.11 mg / TBAI / dimethylformamide / 12 h / 20 °C

With chiral Jacobsen (S,S)-Cr(salen) catalyst; 3-chloro-benzenecarboperoxoic acid; Grubbs catalyst first generation; In dichloromethane;
DOI:10.1016/S0040-4020(03)00857-3