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Water → Methyl 2-[4-(aminomethyl)phenoxy]-2-(2-chlorophenyl)acetate

HRID 257845
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HRID 257845 반응식
[N:1]([CH2:4][C:5]1[CH:23]=[CH:22][C:8]([O:9][CH:10]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[Cl:21])[C:11]([O:13][CH3:14])=[O:12])=[CH:7][CH:6]=1)=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>O1CCCC1>[NH2:1][CH2:4][C:5]1[CH:6]=[CH:7][C:8]([O:9][CH:10]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[Cl:21])[C:11]([O:13][CH3:14])=[O:12])=[CH:22][CH:23]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 11776TriphenylphosphineHCID 19781831HCID 19781831, 화합물

생성물 1

HCID 19781920Methyl 2-[4-(aminomethyl)phenoxy]-2-(2-chlorophenyl)acetate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of the product of Step E in dry tetrahydrofuran is treated protionwise with triphenylphosphine (1 equivalent). The solution is stirred under N2 at ambient temperature. After about 2 hours, when gas evolution has ceased, H2O (1 equivalent) is added, and the solution is concentrated in vacuo, and the residue is chromatographed on silica gel to give the title compound.

후처리

  1. concentrationthe solution is concentrated in vacuo
  2. customthe residue is chromatographed on silica gel

출처 및 근거

ORD 기록
ord-97fa05373712477db9538988520d44fc
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05264439

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