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Hydrochloric Acid → N-[3-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propyl]-acetamide

HRID 1602407
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인쇄 미리보기

반응식

HRID 1602407 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH2:8][CH2:7][C:6]=2[C:10]=1[CH2:11][CH2:12][CH2:13][NH2:14].[C:15](OC(=O)C)(=[O:17])[CH3:16].Cl>N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH2:8][CH2:7][C:6]=2[C:10]=1[CH2:11][CH2:12][CH2:13][NH:14][C:15](=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 7918Acetic AnhydrideHCID 196116373-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propylamine

생성물 1

HCID 19611695N-[3-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propyl]-acetamide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 3-(5-bromo-2,3-dihydro-benzofuran-4-yl)-propylamine (256 mg) in pyridine (3 ml) at 40 was treated with acetic anhydride (0.11 ml) and the solution stored overnight at 4°. The cold solution was acidified with 2N hydrochloric acid and the mixture extracted with ethyl acetate. The extracts were dried and evaporated and the residue chromatographed on silica (20 g) using dichloromethane:methanol:ammonia (100:8:1) to give the title compound as an oil which slowly solidified (175 mg).

후처리

  1. extractionthe mixture extracted with ethyl acetate
  2. customThe extracts were dried
  3. customevaporated
  4. customthe residue chromatographed on silica (20 g)

출처 및 근거

ORD 기록
ord-f16a92737d6e4f218c5560f825517973
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05981572

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