(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester
CAS No.:354153-39-2
Molecular Formula:C₂₇H₃₉NO₅Si
Molecular Weight:485.696
Hs Code.:

Synonyms:(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

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Technology Process of (2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

There total 6 articles about (2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl 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: 92.0%

: 354153-36-9
(S)-6-(tert-butyldiphenylsilanyloxymethyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester

: 354153-39-2
(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With potassium osmate(VI); 4-methylmorpholine N-oxide; In water; acetone;
DOI:10.1016/S0957-4166(01)00136-7

Reference yield:

: 354153-37-0
1,1-dimethylethyl [(1S)-1-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)prop-2-en-1-yl]carbamate

: 354153-39-2
(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluoroacetic acid / CH₂Cl₂ / 1 h / 20 °C

2.1: K₂CO₃ / acetonitrile / 90 °C

3.1: 4.88 g / triethylamine / tetrahydrofuran / 0 - 20 °C

4.1: 97 percent / Grubbs' catalyst / CH₂Cl₂ / 20 °C

5.1: 4-methylmorpholine N-oxide; K₂OsO₄*2H₂O / H₂O; acetone / 20 °C

5.2: 92 percent / Na₂SO₃ / acetone; H₂O

With potassium osmate(VI); potassium carbonate; 4-methylmorpholine N-oxide; triethylamine; trifluoroacetic acid; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; water; acetone; acetonitrile;
DOI:10.1021/jo034137u

Reference yield:

: 354153-38-1
(S)-but-3-enyl[1-(tert-butyldiphenylsilanyloxymethyl)allyl]carbamic acid tert-butyl ester

: 354153-39-2
(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 97 percent / Grubbs' catalyst / CH₂Cl₂ / 20 °C

2.1: 4-methylmorpholine N-oxide; K₂OsO₄*2H₂O / H₂O; acetone / 20 °C

2.2: 92 percent / Na₂SO₃ / acetone; H₂O

With potassium osmate(VI); 4-methylmorpholine N-oxide; Grubbs catalyst first generation; In dichloromethane; water; acetone;
DOI:10.1021/jo034137u