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Carbon tetrabromide → HCID 21349905、化合物

HRID 2186751
ノート
印刷プレビュー

反応式

HRID 2186751 の反応式
O[CH2:2][CH2:3][N:4]1[C:10]2[CH:11]=[CH:12][CH:13]=[C:14]([O:15][CH2:16][C:17]([O:19][CH3:20])=[O:18])[C:9]=2[CH2:8][CH2:7][CH2:6][CH2:5]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Br)(Br)(Br)Br.C(=O)(O)[O-].[Na+].[C:50]1([C:56]([C:59]2[CH:64]=[CH:63][CH:62]=[CH:61][CH:60]=2)([SH:58])[CH3:57])[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1.[H-].[Na+].[Cl-].[NH4+]>C(Cl)Cl.CN(C=O)C>[C:59]1([C:56]([C:50]2[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=2)([S:58][CH2:2][CH2:3][N:4]2[C:10]3[CH:11]=[CH:12][CH:13]=[C:14]([O:15][CH2:16][C:17]([O:19][CH3:20])=[O:18])[C:9]=3[CH2:8][CH2:7][CH2:6][CH2:5]2)[CH3:57])[CH:60]=[CH:61][CH:62]=[CH:63][CH:64]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

10

反応物 7

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 516892Sodium BicarbonateHCID 597528HCID 597528、化合物HCID 21349894HCID 21349894、化合物

生成物 1

HCID 21349905
HCID 21349905、化合物
収率 84.4%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒2 回HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Methyl (1-(2-hydroxyethyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-6-yloxy)acetate (370 mg) was dissolved in methylene chloride (15 ml), and the resultant solution was stirred at 0° C. Triphenylphosphine (1085 mg) and carbon tetrabromide (922 mg) were added to the solution, and the mixture was stirred at 0° C. After disappearance of the raw materials was confirmed, a saturated sodium bicarbonate aqueous solution (15 ml) was added to the reaction solution, and the mixture was then extracted with ethyl acetate. The resultant organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The resultant residue was purified by column chromatography (silica gel:hexane/ethyl acetate=1/1) to obtain a crude product. 1,1-diphenylethanethiol (428 mg) was dissolved in DMF (10 ml) under an argon atmosphere, and the resultant solution was stirred at 0° C. Sodium hydride (65 mg) was added to the solution, and the mixture was stirred at 0° C. for 5 minutes. A solution of the crude product in DMF (3 ml) was added to the mixture at 0° C. After disappearance of the raw materials was confirmed, the reaction solution was added to a saturated ammonium chloride aqueous solution (30 ml), and then extracted with ethyl acetate. The resultant organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The resultant residue was purified by column chromatography (silica gel:hexane/ethyl acetate=8/1) to obtain the object compound (532 mg, yield 84%).

後処理

  1. extractionthe mixture was then extracted with ethyl acetate
  2. washThe resultant organic layer was washed with saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated
  5. customThe resultant residue was purified by column chromatography (silica gel:hexane/ethyl acetate=1/1)
  6. customto obtain a crude product
  7. stirringthe mixture was stirred at 0° C. for 5 minutes
  8. extractionextracted with ethyl acetate
  9. washThe resultant organic layer was washed with saturated brine
  10. dry with materialdried over anhydrous sodium sulfate
  11. concentrationconcentrated
  12. customThe resultant residue was purified by column chromatography (silica gel:hexane/ethyl acetate=8/1)

出典と根拠

ORDレコード
ord-3e4e419d5a4c4aa3b900fdf25079ac5e
出典データセット
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06407096B1

反応ノート

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