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Iodine → 2-Methoxy-pyrrolidine-1-carboxylic acid benzyl ester

HRID 132819
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HRID 132819 반응식
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][C@H:12]1C(O)=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19](OC1C(OC(=O)C)=C(I=O)C=CC=1)(=[O:21])C.II.CO>ClCCl>[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[O:21][CH3:19])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

6

반응물 4

HCID 807IodineHCID 887MethanolHCID 101987Benzyloxycarbonyl-L-prolineHCID 21113495Diacetoxyiodosobenzene

생성물 1

HCID 109224852-Methoxy-pyrrolidine-1-carboxylic acid benzyl ester수율 88.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a mixture of (S)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (purchased at Fluka, Ref 97090, 6 g, 1.0 eq.) in dichloromethane (300 mL) was added diacetoxyiodosobenzene (15.8 g, 2 eq.) and iodine (3.0 eq., 0.5 eq.). The mixture was stirred 5 h at room temperature. Methanol (12 mL) was added and the reaction mixture was stirred for an additional 1.5 h at room temperature, partitioned between an aqueous solution of sodium sulfite and dichloromethane. The organic layer was washed with an aqueous solution of sodium sulfite, brine, evaporated in vacuo and purified on silica eluting with 9:1 cyclohexane/ethyl acetate to yield 5.0 g (88%) of the desired product as light yellow oil. MS (m/e): 235.5 (MH+, 100%)

후처리

  1. stirringthe reaction mixture was stirred for an additional 1.5 h at room temperature
  2. custompartitioned between an aqueous solution of sodium sulfite and dichloromethane
  3. washThe organic layer was washed with an aqueous solution of sodium sulfite, brine
  4. customevaporated in vacuo
  5. custompurified on silica eluting with 9:1 cyclohexane/ethyl acetate

출처 및 근거

ORD 기록
ord-b86cbbeb5da042a2aaf26fadcae3ef6d
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07388095B2

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