ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 1522866
ノート
印刷プレビュー

反応式

HRID 1522866 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-fcf26b0863fe4a148067ba730665034b
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09078871B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート