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Diiodomethane → N-Trifluoroacetyl-1-cyclopropyl-7-ethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine

HRID 84097
ノート
印刷プレビュー

反応式

HRID 84097 の反応式
C([Zn][CH2:4][CH3:5])C.F[C:7](F)(F)[C:8](O)=O.ICI.[F:16][C:17]([F:35])([F:34])[C:18]([N:20]1[CH2:26][C:25](=[CH2:27])[C:24]2[CH:28]=[CH:29][C:30]([O:32]C)=[CH:31][C:23]=2[CH2:22][CH2:21]1)=[O:19]>ClCCl>[F:34][C:17]([F:35])([F:16])[C:18]([N:20]1[CH2:26][CH:25]([CH:27]2[CH2:8][CH2:7]2)[C:24]2[CH:28]=[CH:29][C:30]([O:32][CH2:4][CH3:5])=[CH:31][C:23]=2[CH2:22][CH2:21]1)=[O:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6346DiiodomethaneHCID 6422Trifluoroacetic acidHCID 22292788N-Trifluoroacetyl-7-methoxy-1-methylene 2,3,4,5-tetrahydro-1H-3-benzazepineHCID 178418750HCID 178418750、化合物

生成物 1

HCID 86692803N-Trifluoroacetyl-1-cyclopropyl-7-ethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒
4 回

実験手順

A solution of diethyl zinc (1 mL, 1M in hexanes) in dichloromethane (1 mL) at 0 C was treated with trifluoroacetic acid in dichloromethane (0.5 mL) and the mixture stirred for 15 min. Diiodomethane (0.280 g, 1.0 mmol) in dichloromethane (0.5 mL) was then added and stirred for 15 minutes. N-Trifluoroacetyl-7-methoxy-1-methylene-2,3,4,5-tetrahydro-1H-3-benzazepine (0.075 g, 0.26 mmol) in dichloromethane (1 mL) was added and the mixture stirred for 30 minutes at 0 C and then for 2 hours at 20 C. The product mixture was quenched with aqueous saturated NH4Cl (5 mL), extracted twice with CH2Cl2 (20 mL), washed with saturated aqueous NaHCO3 (10 mL), washed with H2O (10 mL), and concentrated. Flash chromatography (7% EtOAc in hexanes, silica) resulted in 0.050 g of a white solid. MS calculated for C15H16F3NO2+H: 300, observed: 300.

後処理

  1. stirringstirred for 15 minutes
  2. stirringthe mixture stirred for 30 minutes at 0 C
  3. waitfor 2 hours at 20 C
  4. customThe product mixture was quenched with aqueous saturated NH4Cl (5 mL)
  5. extractionextracted twice with CH2Cl2 (20 mL)
  6. washwashed with saturated aqueous NaHCO3 (10 mL)
  7. washwashed with H2O (10 mL)
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-a2a5259243f84507ad3518c5187adba6
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08846906B2

反応ノート

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