HCID 69244338, compound → HCID 69240454, compound

HRID 854670Notes

Reaction equation

HRID 854670 reaction equation
[Si:1]([O:18][C@@H:19]1[CH2:24][CH2:23][CH2:22][C@H:21]([CH2:25][CH:26]=[CH:27][C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[CH2:20]1)([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CO>[Si:1]([O:18][C@@H:19]1[CH2:24][CH2:23][CH2:22][C@H:21]([CH2:25][CH2:26][CH2:27][C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[CH2:20]1)([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 1

HCID 69244338HCID 69244338, compound

Product 1

HCID 69240454HCID 69240454, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

2.4 g of tert-butyl 4-[cis-3-(tert-butyldiphenylsilanyloxy)cyclohexyl]but-2-enoate are dissolved in 35 ml of methanol, and 200 mg of PD (10% on activated carbon) are added. At room temperature, the mixture is stirred under an atmosphere of hydrogen for 7 hours. The catalyst is filtered off through Celite and the filtrate is concentrated under reduced pressure. This gives 2.3 g of tert-butyl 4-[cis-3-(tert-butyldiphenylsilanyloxy)cyclohexyl]-butanoate as an oil. C30H44O3Si (480.75), MS(ESI): 481 (M+H+).

Workup

  1. addition200 mg of PD (10% on activated carbon) are added
  2. filtrationThe catalyst is filtered off through Celite
  3. concentrationthe filtrate is concentrated under reduced pressure

Sources & evidence

ORD record
ord-3f3f402833394c7bb482efeaed6dcc80
Source dataset
uspto-grants-2007_08
Patent number
US07259177B2

Reaction notes

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