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Potassium tert-butoxide → 2-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)anilino]-1,3-oxazol-4-one

HRID 867168
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HRID 867168 반응식
Cl[CH2:2][C:3]([NH:5][C:6]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]([OH:24])([C:20]([F:23])([F:22])[F:21])[C:16]([F:19])([F:18])[F:17])=[CH:11][CH:10]=1)=[O:7])=[O:4].CC(C)([O-])C.[K+]>C(COC)OC>[F:17][C:16]([F:19])([F:18])[C:15]([C:12]1[CH:13]=[CH:14][C:9]([NH:8][C:6]2[O:7][CH2:2][C:3](=[O:4])[N:5]=2)=[CH:10][CH:11]=1)([OH:24])[C:20]([F:23])([F:22])[F:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 23665647Potassium tert-butoxideHCID 538815481-(2-Chloroacetyl)-3-[4-(hexafluoro-2-hydroxy-2-propyl)phenyl] urea

생성물 1

HCID 1785169042-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)anilino]-1,3-oxazol-4-one

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

To 1-(2-chloroacetyl)-3-[4-(hexafluoro-2-hydroxy-2-propyl)phenyl] urea (9.7 gm., 0.026 mole) in dimethoxyethane (500 ml) add potassium t-butoxide (5.7 gm., 0.051 mole). Stir 16 hr., concentrate, add water, acidify with conc. HCl, neutralize with sodium bicarbonate and extract with ether. Dry, concentrate, and recrystallize the residue from ether, to obtain the product, m.p. 272°-274° C.

후처리

  1. concentration, concentrate
  2. additionadd water
  3. extractionextract with ether
  4. customDry
  5. concentrationconcentrate
  6. customrecrystallize the residue from ether
  7. customto obtain the product, m.p. 272°-274° C.

출처 및 근거

ORD 기록
ord-2f44e0ca32b34601b6ac5966e3af761f
출처 데이터셋
uspto-grants-1978_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04103018

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