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Triphenylphosphine → (5S)-5-(aminomethyl)-3-(4-iodophenyl)-1,3-oxazolidin-2-one

HRID 747207
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HRID 747207 반응식
[N:1]([CH2:4][C@@H:5]1[O:9][C:8](=[O:10])[N:7]([C:11]2[CH:16]=[CH:15][C:14]([I:17])=[CH:13][CH:12]=2)[CH2:6]1)=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(#N)C.O>[NH2:1][CH2:4][C@@H:5]1[O:9][C:8](=[O:10])[N:7]([C:11]2[CH:16]=[CH:15][C:14]([I:17])=[CH:13][CH:12]=2)[CH2:6]1
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참가 물질

5

반응물 2

HCID 11776TriphenylphosphineHCID 59749482(5R)-5-(azidomethyl)-3-(4-iodophenyl)-1,3-oxazolidin-2-one

생성물 1

HCID 59749453(5S)-5-(aminomethyl)-3-(4-iodophenyl)-1,3-oxazolidin-2-one수율 81.3%

시약·촉매·용매 2

HCID 962Water용매HCID 6342Acetonitrile용매

실험 절차

(5R)-5-(Azidomethyl)-3-(4-Iodophenyl)-1,3-oxazolidin-2-one (8.0 g, 23.2 mmol) was dissolved in acetonitrile (160 ml) and water (16 ml). Triphenylphosphine (7.3 g, 27.9 mmol) was added and the mixture stirred at room temperature overnight. The volatiles were removed by concentration in vacuo, and the resulting residue partitioned between water (200 ml) and dichloromethane (200 ml). The aqueous layer was extracted with dichloromethane (2×200 ml) and dried over sodium sulfate. The crude material was purified by flash chromatography on silica gel with 0-10% methanol in dichloromethane as the eluent giving the desired product (6.0 g).

후처리

  1. customThe volatiles were removed by concentration in vacuo
  2. customthe resulting residue partitioned between water (200 ml) and dichloromethane (200 ml)
  3. extractionThe aqueous layer was extracted with dichloromethane (2×200 ml)
  4. dry with materialdried over sodium sulfate
  5. customThe crude material was purified by flash chromatography on silica gel with 0-10% methanol in dichloromethane as the eluent

출처 및 근거

ORD 기록
ord-9e7136d470a34d3e8cc4abe079542255
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07396847B2

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