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Water → 5-Keto Vioxx

HRID 1458319
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HRID 1458319 반응식
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:7][CH:6]=1)(=[O:4])=[O:3].C(O[C:18](=O)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=O.[K].O.C[C:29](OC(C)=O)=[O:30]>>[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([C:11]2[C:12]([O:14][C:29](=[O:30])[C:18]=2[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)=[O:13])=[CH:9][CH:10]=1)(=[O:3])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 962WaterHCID 7918Acetic Anhydride2회HCID 5723454-Mesylphenylacetic acidHCID 86753446HCID 86753446, 화합물

생성물 1

HCID 121856695-Keto Vioxx

실험 절차

A mixture of 21.4 g (0.10 mol) of 4-(methylsulfonyl) phenylacetic acid [Forrest, et al., J. Chem. Soc. (1948), 1501-1506] and 18.8 g (0.10 mol) of potassium benzoyl formate in 200 mL of Ac2O is stirred and refluxed for 2 h. The reaction mixture is cooled to r.t. and poured into 1L of H2O and stirred until the Ac2O dissolves (ca. 2h). The precipitate is filtered and dried to obtain the title compound. If desired, it is recrystallized from HOAc or acetone.

후처리

  1. temperaturerefluxed for 2 h
  2. filtrationThe precipitate is filtered
  3. customdried

출처 및 근거

ORD 기록
ord-892bcb193de04e209fda8d95492084d6
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05849943

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