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Water → HCID 86638598、化合物

HRID 1677848
ノート
印刷プレビュー

反応式

HRID 1677848 の反応式
[H-].[Na+].[O:3]1[C:7]2([CH2:11][CH2:10][N:9]([C@H:12]3[CH2:17][CH2:16][CH2:15][CH2:14][C@@H:13]3[OH:18])[CH2:8]2)[O:6][CH2:5][CH2:4]1.[CH:19]1([CH2:25][CH2:26][CH2:27]Br)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1.O>CN(C)C=O>[O:6]1[C:7]2([CH2:11][CH2:10][N:9]([C@H:12]3[CH2:17][CH2:16][CH2:15][CH2:14][C@@H:13]3[O:18][CH2:27][CH2:26][CH2:25][CH:19]3[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)[CH2:8]2)[O:3][CH2:4][CH2:5]1
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 962WaterHCID 24758Sodium hydrideHCID 96426(3-Bromopropyl)cyclohexaneHCID 16738222HCID 16738222、化合物

生成物 1

HCID 86638598HCID 86638598、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒3 回

実験手順

To a suspension of sodium hydride (200 mg, 8.33 mmol) in anhydrous dimethylformamide (20 mL) was added a solution of (1R,2R)/(1S,2S)-2-(1,4-dioxa-7-azaspiro[4.4]non-7-yl)cyclohexanol (1.5 g, 6.6 mmol) in anhydrous dimethylformamide (10 mL). The resulting mixture was stirred at room temperature for 30 min. and then a solution of 3-(cyclohexyl)propyl bromide (1.67 g, 8.15 mmols) in anhydrous dimethylformamide was quickly added. The reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was poured into water (200 mL) and then extracted with ethyl acetate (3×50 mL). The combined organic extracts were back-washed with brine (50 mL) and the solvent was evaporated in vacuo. The residue was taken up with water (50 mL) and the pH was adjusted to pH 1.0 with 6M HCl aqueous solution. The acidic aqueous solution was extracted with diethyl ether (2×50 mL), then basified to pH 5.0-5.5 with 5M NaOH aqueous solution and extracted with diethyl ether (3×50 mL). The combined organic extracts at pH 5.0-5.5 were concentrated in vacuo to provide the crude title compound suitable for the next step without any further purification.

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 16 hours
  2. extractionextracted with ethyl acetate (3×50 mL)
  3. washThe combined organic extracts were back-washed with brine (50 mL)
  4. customthe solvent was evaporated in vacuo
  5. extractionThe acidic aqueous solution was extracted with diethyl ether (2×50 mL)
  6. extractionextracted with diethyl ether (3×50 mL)
  7. concentrationThe combined organic extracts at pH 5.0-5.5 were concentrated in vacuo

出典と根拠

ORDレコード
ord-eee44ac5d56b4b87b77c890dd3c61c8b
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08008342B2

反応ノート

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