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Diethyl Ether → Acridine-9-carbonyl chloride hydrochloride

HRID 2256800
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HRID 2256800 반응식
O.[CH:2]1[C:15]2[C:6](=[N:7][C:8]3[C:13]([C:14]=2[C:16]([OH:18])=O)=[CH:12][CH:11]=[CH:10][CH:9]=3)[CH:5]=[CH:4][CH:3]=1.C(OCC)C.S(Cl)([Cl:26])=O>>[ClH:26].[CH:2]1[C:15]2[C:6](=[N:7][C:8]3[C:13]([C:14]=2[C:16]([Cl:26])=[O:18])=[CH:12][CH:11]=[CH:10][CH:9]=3)[CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 3283Diethyl EtherHCID 24386Thionyl ChlorideHCID 162116879-Acridinecarboxylic Acid Hydrate

생성물 1

HCID 12395930Acridine-9-carbonyl chloride hydrochloride수율 100%

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온도
100 °C

실험 절차

A mixture of 9-acridinecarboxylic acid hydrate (10.0 g, 44.80 mmol) in 80 mL of thionyl chloride was refluxed at 100° C. under nitrogen for 2 hours, and then cooled to 25° C. The resulting solution was reduced to about half the original volume under reduced pressure, and then poured into 500 mL of anhydrous diethyl ether. The yellow precipitate was collected, washed with ether (3×100 mL), and dried under reduced pressure for 2 hours, to produce 12.95 g (~ 100% yield) of the product, which was used immediately for the next reaction.

후처리

  1. temperaturecooled to 25° C
  2. customThe yellow precipitate was collected
  3. washwashed with ether (3×100 mL)
  4. customdried under reduced pressure for 2 hours

출처 및 근거

ORD 기록
ord-b93f61a3cba441c89a839d80d6415607
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05656426

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