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Hydrochloric Acid → HCID 23468307, 화합물

HRID 443654
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HRID 443654 반응식
[C:1]1([O:11][CH2:12][CH2:13][NH:14][C:15]2[CH:23]=[CH:22][C:18]([C:19]([OH:21])=[O:20])=[CH:17][CH:16]=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[C:24](Cl)(=[O:26])[CH3:25].Cl>N1C=CC=CC=1>[C:24]([N:14]([CH2:13][CH2:12][O:11][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1)[C:15]1[CH:16]=[CH:17][C:18]([C:19]([OH:21])=[O:20])=[CH:22][CH:23]=1)(=[O:26])[CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6367Acetyl chlorideHCID 23468289HCID 23468289, 화합물

생성물 1

HCID 23468307HCID 23468307, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 6.14 g. of 4-[2-(1-naphthyloxy)ethylamino]benzoic acid and 20 ml. of acetyl chloride in 50 ml. pyridine is warmed on a steam-bath for 8 hours. The dark solution is then poured into 370 ml. of 2 N hydrochloric acid. The resulting solution is then extracted several times with methylene chloride. The residue from evaporation of this extract is crystallized from acetonitrile giving a white solid, m.p. 182°-183° C.

후처리

  1. additionThe dark solution is then poured into 370 ml
  2. extractionThe resulting solution is then extracted several times with methylene chloride
  3. customThe residue from evaporation of this extract
  4. customis crystallized from acetonitrile giving a white solid, m.p. 182°-183° C.

출처 및 근거

ORD 기록
ord-9139bd0a73e84edcb3bcb1fe8a43fe45
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04260816

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