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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → 20290-48-6

HRID 974803
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반응식

HRID 974803 반응식
C1C=C(Cl)C=C(C(OO)=[O:9])C=1.[CH:12]1[C:17]2[C:18](=[O:27])[NH:19][C:20]3[CH:26]=[CH:25][CH:24]=[CH:23][C:21]=3[S:22][C:16]=2[CH:15]=[CH:14][CH:13]=1.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl>[CH:12]1[C:17]2[C:18](=[O:27])[NH:19][C:20]3[CH:26]=[CH:25][CH:24]=[CH:23][C:21]=3[S:22](=[O:9])[C:16]=2[CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70297m-Chloroperbenzoic acidHCID 374829DibenzothiazepinoneHCID 516892Sodium Bicarbonate

생성물 1

HCID 1300037220290-48-6

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

A solution of MCPBA (1 eq) in chloroform (5 ml) was added to a stirred solution of 10,11-dihydrodibenzo[b,f][1,4] thiazepin-11-one (114 mg, 0.5 mmol) in chloroform (30 ml). After 0.5 hr the reaction mixture was poured into sodium bicarbonate solution (5%, 30 ml), separated and the aqueous layer washed with chloroform (30 ml). The combined organic fractions were dried (MgSO4) and evaporated. Recrystallisation from toluene gave the title compound as off-white crystals (76 mg, m.p. 308°-310° C., Rf 0.16, CH2Cl2 /MeOH 50:1).

후처리

  1. customseparated
  2. washthe aqueous layer washed with chloroform (30 ml)
  3. dry with materialThe combined organic fractions were dried (MgSO4)
  4. customevaporated
  5. customRecrystallisation from toluene

출처 및 근거

ORD 기록
ord-591f3b49902d4942af36c3b9b0e0f97d
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05607929

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