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

HRID 2368913
ノート
印刷プレビュー

反応式

HRID 2368913 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-5d6f2a35673a4b468cac7794bd9a9344
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08703810B2

反応ノート

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