Ammonia → 4-Benzofuranacetamide

HRID 751491노트

반응식

HRID 751491 반응식
C(N1C=CN=C1)([N:3]1C=CN=C1)=O.[O:13]1[C:17]2[CH:18]=[CH:19][CH:20]=[C:21]([CH2:22][C:23]([OH:25])=O)[C:16]=2[CH:15]=[CH:14]1.N>O1CCCC1>[O:13]1[C:17]2[CH:18]=[CH:19][CH:20]=[C:21]([CH2:22][C:23]([NH2:3])=[O:25])[C:16]=2[CH:15]=[CH:14]1

참가 물질

5

반응물 3

HCID 222AmmoniaHCID 682631,1'-CarbonyldiimidazoleHCID 27675512-(1-Benzofuran-4-yl)acetic acid

생성물 1

HCID 179764934-Benzofuranacetamide수율 93%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
20 °C

실험 절차

Add 1,1′-carbonyldiimidazole (2.3 g, 14.2 mmol) to a solution of benzofur-4-ylacetic acid (2.5 g, 14.2 mmol) in anhydrous tetrahydrofuran (12 mL) under nitrogen and stir at 20° C. for 4 hours. Bubble anhydrous ammonia through the solution, dilute with anhydrous tetrahydrofuran (10 mL), and stir at 20° C. for 18 hours. Concentrate under reduced pressure, and wash the solid with aqueous sodium hydrogen sulfate and distilled water. Dry under vacuum to obtain 2.3 g (93%) of the title compound as a pale yellow solid. Mass spectrum (ES, m/z) (M+H)=176.1.

후처리

  1. stirringstir at 20° C. for 18 hours
  2. concentrationConcentrate under reduced pressure
  3. washwash the solid with aqueous sodium hydrogen sulfate
  4. distillationdistilled water
  5. customDry under vacuum

출처 및 근거

ORD 기록
ord-7056da19d96a4a7caac1121624ce544c
출처 데이터셋
uspto-grants-2008_07
특허 번호
US07405305B2

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