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Thionyl Chloride → HCID 87822203, 화합물

HRID 916552
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HRID 916552 반응식
[CH:1]1[C:13]2[CH:12]([CH2:14][CH2:15][N:16]([CH3:22])[CH2:17][CH2:18][C:19](O)=[O:20])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:25])=O>ClC(Cl)C>[ClH:25].[CH:1]1[C:13]2[CH:12]([CH2:14][CH2:15][N:16]([CH3:22])[CH2:17][CH2:18][C:19]([Cl:25])=[O:20])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 69412355HCID 69412355, 화합물

생성물 1

HCID 87822203HCID 87822203, 화합물

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

실험 절차

A solution of 3-{[2-(9H-fluoren-9-yl)-ethyl]-methyl-amino}-propionic acid (11.4 g) in dichloroethane (115 ml) is treated with thionyl chloride (7.71 g) at room temperature for 5′ and at 60° for 1 hour. About 20 ml volatiles are removed under reduced pressure. 100 ml diethyl ether are added and the mixture kept at 5° over night for crystallization. The crystals are collected by filtration, washed with dichloroethane/diethylether and dried. M.p. 120°-123°.

후처리

  • customAbout 20 ml volatiles are removed under reduced pressure
  • addition100 ml diethyl ether are added
  • customthe mixture kept at 5° over night for crystallization
  • filtrationThe crystals are collected by filtration
  • washwashed with dichloroethane/diethylether
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-fed1982e821e4313b131f928af7c5078
    출처 데이터셋
    uspto-grants-2007_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07271168B2

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