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t-Butyl 3-methoxy-4-o-tolylureidophenylacetate → 3-Methoxy-4-o-tolylureidophenylacetic acid

HRID 381253
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인쇄 미리보기

반응식

HRID 381253 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:20][C:21]([O:23]C(C)(C)C)=[O:22])[CH:6]=[CH:7][C:8]=1[NH:9][C:10]([NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH3:19])=[O:11]>FC(F)(F)C(O)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:20][C:21]([OH:23])=[O:22])[CH:6]=[CH:7][C:8]=1[NH:9][C:10]([NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH3:19])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 69645017t-Butyl 3-methoxy-4-o-tolylureidophenylacetate

생성물 1

HCID 114498403-Methoxy-4-o-tolylureidophenylacetic acid수율 100%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of t-butyl 3-methoxy-4-o-tolylureidophenylacetate (0.016 g, 0.043 mmol) in trifluoroacetic acid (1.0 mL) was stirred for 1 h. The reaction was concentrated and the residue coevaporated with methylene chloride (2×) then ether to afford 3-methoxy-4-o-tolylureidophenylacetic acid (0.0135 g, 100%) as a white residue.

후처리

  1. concentrationThe reaction was concentrated

출처 및 근거

ORD 기록
ord-2e9aebfce6e34a6c8a11410be9a8e6e7
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06306840B1

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