(-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

Base Information

Chemical Name:(-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine
CAS No.:229170-68-7
Molecular Formula:C₂₅H₃₇NO₄Si
Molecular Weight:443.659
Hs Code.:

Synonyms:(-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

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Chemical Property of (-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

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Technology Process of (-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

There total 5 articles about (-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine 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: 99.0%

: 501-53-1,94274-21-2
benzyl chloroformate

: 229170-67-6
(-)-(2R,3R,6S)-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

: 229170-68-7
(-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

Guidance literature:: With potassium carbonate; In water; acetonitrile; for 4h;
DOI:10.1021/jo9823240

Reference yield:

: 209160-33-8
(+)-(2S,5S,6R)-1-aza-2-(3-furyl)-5-methyl-8-oxa-4,9-dioxobicyclo[4.3.0]nonane

: 229170-68-7
(-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

Guidance literature:: Multi-step reaction with 5 steps

1: 96 percent / lithium hexamethyldisilylamide / tetrahydrofuran / 1.5 h / -80 °C

2: 89 percent / hydrogen / PtO₂ / ethanol / 8 h / 20 °C

3: 95 percent / t-BuOK / tetrahydrofuran / 0.5 h / 0 °C

4: 67 percent / imidazole / acetonitrile / 4 h / 20 °C

5: 99 percent / K₂CO₃ / acetonitrile; H₂O / 4 h

With 1H-imidazole; potassium tert-butylate; hydrogen; potassium carbonate; lithium hexamethyldisilazane; platinum(IV) oxide; In tetrahydrofuran; ethanol; water; acetonitrile; 1: Addition / 2: Hydrogenation / 3: Ring cleavage / 4: Etherification / 5: Substitution;
DOI:10.1021/jo9823240

Reference yield:

: 229170-66-5
Trifluoro-methanesulfonic acid (5S,8S,8aR)-5-furan-3-yl-8-methyl-3-oxo-1,5,8,8a-tetrahydro-oxazolo[3,4-a]pyridin-7-yl ester

: 229170-68-7
(-)-(2R,3R,6S)-N-benzyloxycarbonyl-2-(tert-butyldimethylsilyloxymethyl)-6-(3-furyl)-3-methylpiperidine

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / hydrogen / PtO₂ / ethanol / 8 h / 20 °C

2: 95 percent / t-BuOK / tetrahydrofuran / 0.5 h / 0 °C

3: 67 percent / imidazole / acetonitrile / 4 h / 20 °C

4: 99 percent / K₂CO₃ / acetonitrile; H₂O / 4 h

With 1H-imidazole; potassium tert-butylate; hydrogen; potassium carbonate; platinum(IV) oxide; In tetrahydrofuran; ethanol; water; acetonitrile; 1: Hydrogenation / 2: Ring cleavage / 3: Etherification / 4: Substitution;
DOI:10.1021/jo9823240