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Triethylamine → 1-(Chloromethyl)-4-methoxy-2-methylbenzene

HRID 1522866
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HRID 1522866 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9]O)=[C:5]([CH3:11])[CH:4]=1.C(N(CC)CC)C.CS([Cl:23])(=O)=O>C1(C)C=CC=CC=1>[Cl:23][CH2:9][C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][C:5]=1[CH3:11]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 27595864-Methoxy-2-methylbenzyl alcohol

생성물 1

HCID 110520871-(Chloromethyl)-4-methoxy-2-methylbenzene

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of (4-methoxy-2-methylphenyl)methanol (8.2 g, 54.0 mmol) and triethylamine (9.1 mL, 65.0 mmol) in toluene (100 mL) at 0° C., methanesulfonyl chloride (5.1 mL, 65.0 mmol) was added via syringe over 20 min. The ice water bath was removed, and the reaction was allowed to stir at room temperature for 30 min, heated at 80° C. for 3 days, and then concentrated. The reaction was diluted with DCM, washed with H2O (3×100 mL) and brine, dried over Na2SO4, and concentrated under reduced pressure to 1-(chloromethyl)-4-methoxy-2-methylbenzene (8.1 g) as a dark brown oil. 1H NMR (300 MHz, CDCl3): δ 7.25 (d, 1H), 6.75 (m, 2H), 4.62 (s, 2H), 3.82 (s, 3H), 2.43 (s, 3H).

후처리

  1. customThe ice water bath was removed
  2. temperatureheated at 80° C. for 3 days
  3. concentrationconcentrated
  4. additionThe reaction was diluted with DCM
  5. washwashed with H2O (3×100 mL) and brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated under reduced pressure to 1-(chloromethyl)-4-methoxy-2-methylbenzene (8.1 g) as a dark brown oil

출처 및 근거

ORD 기록
ord-fcf26b0863fe4a148067ba730665034b
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09078871B2

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