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Water → 2-(7-Hydroxyheptyl)isoindoline-1,3-dione

HRID 1911497
ノート
印刷プレビュー

反応式

HRID 1911497 の反応式
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][OH:9].[C:10](=[NH:21])([O-:20])[C:11]1[C:12](=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:13](=N)[O-:14].[K+].[K+].O.C(Cl)Cl>CN(C=O)C>[OH:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:21]1[C:10](=[O:20])[C:11]2[C:12](=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:13]1=[O:14]
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 6344DichloromethaneHCID 662841-Heptanol, 7-bromo-HCID 86762179HCID 86762179、化合物

生成物 1

HCID 189709042-(7-Hydroxyheptyl)isoindoline-1,3-dione

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

585 mg of 7-bromoheptanol was dissolved in 5 mL of DMF. 833 mg of potassium phthalimidate was added, and the mixture was stirred for 4 h. 50 mL of water and 50 mL of DCM were added to the reaction system, which was violently vibrated and then isolated. The water layer was once again extracted with 50 mL of DCM. The two organic layers were combined, successively washed with 100 mL of water and 100 mL of saturated sodium chloride aqueous solution, dried over 5 g of anh. MgSO4 for 30 min, and concentrated via a rotary evaporator to obtain a pale yellow transparent oily liquid.

後処理

  1. customisolated
  2. extractionThe water layer was once again extracted with 50 mL of DCM
  3. washsuccessively washed with 100 mL of water and 100 mL of saturated sodium chloride aqueous solution
  4. dry with materialdried over 5 g of anh. MgSO4 for 30 min
  5. concentrationconcentrated via a rotary evaporator
  6. customto obtain a pale yellow transparent oily liquid

出典と根拠

ORDレコード
ord-5a3cdb369ff64d53b4918e28170bd089
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08604065B2

反応ノート

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