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Benzyl Chloride → Methyl 3-(aminomethyl)-4-hydroxycyclopentane-1-carboxylate

HRID 2244678
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HRID 2244678 반응식
[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH:8]([OH:10])[CH:7]([C:11]#[N:12])[CH2:6]1)=[O:4].C(Cl)C1C=CC=CC=1>CO.C([O-])(O)=O.[Na+].[Pd]>[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH:8]([OH:10])[CH:7]([CH2:11][NH2:12])[CH2:6]1)=[O:4]
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참가 물질

6

반응물 2

HCID 7503Benzyl ChlorideHCID 68685924(1SR,3RS,4SR)-3-cyano-4-hydroxy-cyclopentanecarboxylic acid methyl ester

생성물 1

HCID 68685423Methyl 3-(aminomethyl)-4-hydroxycyclopentane-1-carboxylate수율 99.8%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매
HCID 516892
Sodium Bicarbonate
용매

실험 절차

To a stirred solution of (1SR,3SR,4RS)-3-cyano-4-hydroxy-cyclopentanecarboxylic acid methyl ester (185 mg) at r.t. in methanol (5 ml) under an argon atmosphere were added benzyl chloride (0.38 ml) and 10% Pd/C (50 mg). The mixture was stirred at r.t. under a hydrogen atmosphere (balloon) overnight. The catalyst was filtered off and washed with methanol. The filtrate was concentrated to leave a brown viscous oil. This was taken up in 10 ml sat. aq. NaHCO3 and extracted with CH2Cl2/MeOH 9:1 (3×10 ml) and CH2Cl2/MeOH 4:1 (10 ml). A white solid started to precipitate out of the biphasic mixture which was filtered off. The filtrate was neutralized by the addition of 1 N HCl and concentrated to leave crude (1SR,3SR,4RS)-3-aminomethyl-4-hydroxy-cyclopentane-carboxylic acid methyl ester as a light brown solid (189 mg).

후처리

  1. filtrationThe catalyst was filtered off
  2. washwashed with methanol
  3. concentrationThe filtrate was concentrated
  4. customto leave a brown viscous oil
  5. extractionextracted with CH2Cl2/MeOH 9:1 (3×10 ml) and CH2Cl2/MeOH 4:1 (10 ml)
  6. customto precipitate out of the biphasic mixture which
  7. filtrationwas filtered off
  8. additionThe filtrate was neutralized by the addition of 1 N HCl
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9544c6b36b434cea8cb3fce49b6303d5
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07678917B2

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