Dimethylformamide → 6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione

HRID 456355

反応式

HRID 456355 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9](=[O:11])[NH:8][C:7](=[O:12])[C:6]=2[CH:13]=1.CN(C=O)C.[Br:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]Br.C(N(C(C)C)CC)(C)C>O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9](=[O:11])[N:8]([CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][Br:19])[C:7](=[O:12])[C:6]=2[CH:13]=1

参加物

6

反応物 4

HCID 6228Dimethylformamide2 回HCID 81531DiisopropylethylamineHCID 903596-Chloro-2h-1,3-benzoxazine-2,4(3h)-dioneHCID 2214831,10-Dibromodecane

生成物 1

HCID 222514226-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione収率 49.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A slurry of 9.77 g of 6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione (50 mmol) and 60 ml of DMF was treated with a solution of 1,10-dibromodecane (52.52 g, 0.175 mol) and DMF (60 ml) was added. Diisopropylethylamine (9.6 ml, 55 mmol) was added dropwise. A thermometer and condenser were attached, and the flask was placed in an oil bath. The reaction was heated to 60 C. for approximately 3 hrs, cooled to 47 C. and hexanes (150 ml) were added. The mixture was diluted with water (175 ml). The resulting solids were removed by filtration. The aqueous layer was washed with warm hexanes. The resulting solids were filtered from the hexane layer and recrystallized from warm hexanes to give 10.39 g of 6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione.

後処理

  1. additionwas added
  2. customthe flask was placed in an oil bath
  3. temperatureThe reaction was heated to 60 C
  4. temperaturecooled to 47 C
  5. customThe resulting solids were removed by filtration
  6. washThe aqueous layer was washed with warm hexanes
  7. filtrationThe resulting solids were filtered from the hexane layer
  8. customrecrystallized
  9. temperaturefrom warm hexanes

出典と根拠

ORDレコード
ord-3eb9aa6ce62546f78904c2eb2703b578
出典データセット
uspto-grants-2007_03
特許番号
US07186414B2

関連ノート

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