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2-Bromo-4-chloro-1-phenylbutan-1-one → HCID 54145555, 화합물

HRID 460767
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인쇄 미리보기

반응식

HRID 460767 반응식
[C:1]([CH:9](Br)[CH2:10][CH2:11][Cl:12])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:14][NH:15][C:16](=[S:18])[S-:17].C[NH3+]>>[CH3:14][N:15]1[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:9]([CH2:10][CH2:11][Cl:12])[S:18][C:16]1=[S:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 202266952-Bromo-4-chloro-1-phenylbutan-1-oneHCID 7355561921160-95-2

생성물 1

HCID 54145555HCID 54145555, 화합물

실험 절차

The 3-methyl-4-phenyl-5-β-chloroethyl-4-thiazoline-2-thione is prepared in the following manner: A solution of 33 g of 1-benzoyl-1-bromo-3-chloropropane in 150 cc of absolute alcohol is added slowly to a suspension of 20 g of methyl ammonium N-methyldithiocarbamate in 150 cc of absolute alcohol. The mixture is agitated for 2 hours at ambient temperature and the solvent is then evaporated under reduced pressure. The residue is redissolved in chloroform, washed with water and the separated organic phase is dried over Na2SO4 and then evaporated to dryness.

후처리

  1. customthe solvent is then evaporated under reduced pressure
  2. dissolutionThe residue is redissolved in chloroform
  3. washwashed with water
  4. dry with materialthe separated organic phase is dried over Na2SO4
  5. custom
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
evaporated to dryness

출처 및 근거

ORD 기록
ord-89af0c251e0f45e1ab599a0d8ab0932f
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04061637

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