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Methanol → HCID 66718521、化合物

HRID 515490
ノート
印刷プレビュー

反応式

HRID 515490 の反応式
COC1C=CC(C[N:8]2[CH2:14][CH2:13][CH2:12][O:11][CH:10]([CH3:15])[CH2:9]2)=CC=1.[Cl:18]C(OC(Cl)C)=O.CO>ClCCCl>[ClH:18].[CH3:15][CH:10]1[CH2:9][NH:8][CH2:14][CH2:13][CH2:12][O:11]1
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 887MethanolHCID 5213051-Chloroethyl chloroformateHCID 67281011HCID 67281011、化合物

生成物 1

HCID 66718521HCID 66718521、化合物収率 90.2%

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

To a solution of 4-(4-methoxy-benzyl)-2-methyl-[1,4]oxazepane (1.66 g, 7.05 mmol) in 1,2-dichloroethane (12 ml) was added 1-chloroethyl chloroformate (2.52 g, 17.6 mmol) at room temperature. The mixture was refluxed for 5 hours and cooled to room temperature. After the addition of methanol (15 ml), the mixture was refluxed for 3 hours and concentrated in vacuo to afford the crude product. This crude product was partitioned between ether and 1N hydrochloric acid, and washed with ether. The water phase was basified with saturated aqueous sodium hydrogen carbonate. The product was extracted with dichloromethane. The organic layer was dried over sodium sulfate and the solvent was removed under reduced pressure carefully to avoid evaporating the product. To the resulting solution was added 4N hydrochloric acid in ethyl acetate. The solution was concentrated in vacuo to afford 2-methyl-[1,4]oxazepane hydrochloride as pale yellow oil (964 mg, 90%).

後処理

  1. temperatureThe mixture was refluxed for 5 hours
  2. temperaturethe mixture was refluxed for 3 hours
  3. concentrationconcentrated in vacuo
  4. customto afford the crude product
  5. customThis crude product was partitioned between ether and 1N hydrochloric acid
  6. washwashed with ether
  7. extractionThe product was extracted with dichloromethane
  8. dry with materialThe organic layer was dried over sodium sulfate
  9. customthe solvent was removed under reduced pressure carefully
  10. customto avoid evaporating the product
  11. additionTo the resulting solution was added 4N hydrochloric acid in ethyl acetate
  12. concentrationThe solution was concentrated in vacuo

出典と根拠

ORDレコード
ord-5a88eed17aa6454c84ca2c19acb9cb3c
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09108957B2

反応ノート

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