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Triethylamine → 4-Methanesulfonyl-6-methyl-3,4-dihydro-2H-benzo[1,4]oxazine

HRID 1295557
ノート
印刷プレビュー

反応式

HRID 1295557 の反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][CH2:8][NH:7][C:6]=2[CH:11]=1.C(N(CC)CC)C.[CH3:19][S:20](Cl)(=[O:22])=[O:21]>ClCCl>[CH3:19][S:20]([N:7]1[C:6]2[CH:11]=[C:2]([CH3:1])[CH:3]=[CH:4][C:5]=2[O:10][CH2:9][CH2:8]1)(=[O:22])=[O:21]
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 6494096-methyl-3,4-dihydro-2H-1,4-benzoxazine

生成物 1

HCID 694178614-Methanesulfonyl-6-methyl-3,4-dihydro-2H-benzo[1,4]oxazine収率 93%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

6-Methyl-3,4-dihydro-2H-benzo[1,4]oxazine (1.49 g, 10 mmol) was dissolved in dichloromethane (50 mL) and treated with triethylamine (1.14 g, 11 mmol) followed by the dropwise addition of methanesulfonyl chloride (1.26 g, 11 mmol). The mixture was stirred at ambient temperature for 18 h then evaporated to dryness under reduced pressure. The residue was partitioned between ethyl acetate and saturated aqueous NaHCO3. The phases were separated and the organic phase washed with water, saturated brine, dried (MgSO4) and evaporated to dryness under reduced pressure to give the title compound (2.09 g, 93%) as a brown solid.

後処理

  1. customthen evaporated to dryness under reduced pressure
  2. customThe residue was partitioned between ethyl acetate and saturated aqueous NaHCO3
  3. customThe phases were separated
  4. washthe organic phase washed with water, saturated brine
  5. dry with materialdried (MgSO4)
  6. customevaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-028e2a324f354eb7aea644437ba0f178
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07244726B2

反応ノート

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