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Carbon Tetrachloride → 2-Methyl-5-phenylbenzyl chloride

HRID 1883639
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인쇄 미리보기

반응식

HRID 1883639 반응식
[CH3:1][C:2]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:3]=1[CH2:4]O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Cl)(Cl)(Cl)[Cl:36]>>[CH3:1][C:2]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:3]=1[CH2:4][Cl:36]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 5943Carbon TetrachlorideHCID 11776TriphenylphosphineHCID 12056528(4-Methylbiphenyl-3-yl)methanol

생성물 1

HCID 235082292-Methyl-5-phenylbenzyl chloride

실험 절차

500 mg (2.52 mmol) of 2-methyl-5-phenylbenzyl alcohol (produced in the same manner as in Reference Production Example 1 (4)) was dissolved in 2 ml of carbon tetrachloride, and to this solution was added 1.0 g (3.28 mmol) of triphenylphosphine under nitrogen atmosphere. The reaction mixture was stirred for 1.5 hours under reflux with heating, cooled to room temperature, then, concentrated. The residue was subjected to silica gel column chromatography (eluant: hexane/ethyl acetate=10/1 (v/v)), to obtain 508 mg of 2-methyl-5-phenylbenzyl chloride.

후처리

  • temperatureunder reflux
  • temperaturewith heating
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-a2993cb00ac24ccaa4d4efdfa25b68a4
    출처 데이터셋
    uspto-grants-2004_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06762197B2

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