(2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine

Base Information

• Chemical Name: (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine
• CAS No.: 441310-85-6
• Molecular Formula: C₄₃H₄₉NO₄Si
• Molecular Weight: 671.952
• Mol file: 441310-85-6.mol

Synonyms:(2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine

Chemical Property of (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine

There total 10 articles about (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine 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: 82.0%

(2S,3R,4R,5S)-1-Allyl-3,4,5-tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine (441310-84-5) → (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine (441310-85-6)

Guidance literature:

(2S,3R,4R,5S)-1-Allyl-3,4,5-tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine; With carbonochloridic acid 1-chloro-ethyl ester; In 1,2-dichloro-ethane; at 90 ℃; for 24h;

With methanol; at 80 ℃; for 21h;

DOI:10.1016/S0040-4039(02)00250-2

Reference yield:

benzyl bromide (100-39-0) → (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine (441310-85-6)

Guidance literature:

Multi-step reaction with 6 steps

1.1: 85 percent / NaH; 18-crown-6 / tetrahydrofuran / 19 h / 70 °C

2.1: 70 percent / NBS / acetonitrile; H₂O / 2 h

3.1: 92 percent / NaBH₄ / ethanol / 20 h

4.1: 80 percent / Et₃N; DMAP / CH₂Cl₂ / 3 h / -15 °C

5.1: 73 percent / 39 h / 70 °C

6.1: ACE-Cl / 1,2-dichloro-ethane / 24 h / 90 °C

6.2: 82 percent / MeOH / 21 h / 80 °C

With dmap; sodium tetrahydroborate; N-Bromosuccinimide; 18-crown-6 ether; carbonochloridic acid 1-chloro-ethyl ester; sodium hydride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; 1,2-dichloro-ethane; acetonitrile;

DOI:10.1016/S0040-4039(02)00250-2

Reference yield:

pent-4-enyl α,β-D-glucopyranoside (182074-52-8) → (2S,3R,4R,5S)-3,4,5-Tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine (441310-85-6)

Guidance literature:

Multi-step reaction with 7 steps

1.1: 94 percent / DBU / tetrahydrofuran / 22 h

2.1: 85 percent / NaH; 18-crown-6 / tetrahydrofuran / 19 h / 70 °C

3.1: 70 percent / NBS / acetonitrile; H₂O / 2 h

4.1: 92 percent / NaBH₄ / ethanol / 20 h

5.1: 80 percent / Et₃N; DMAP / CH₂Cl₂ / 3 h / -15 °C

6.1: 73 percent / 39 h / 70 °C

7.1: ACE-Cl / 1,2-dichloro-ethane / 24 h / 90 °C

7.2: 82 percent / MeOH / 21 h / 80 °C

With dmap; sodium tetrahydroborate; N-Bromosuccinimide; 18-crown-6 ether; carbonochloridic acid 1-chloro-ethyl ester; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; 1,2-dichloro-ethane; acetonitrile;

DOI:10.1016/S0040-4039(02)00250-2

upstream raw materials:

(2S,3R,4R,5S)-1-Allyl-3,4,5-tris-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-piperidine

benzyl bromide

pent-4-enyl α,β-D-glucopyranoside

pent-4-enyl 6-O-tert-butyldiphenylsilyl-D-glucopyranoside