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

HRID 1911497
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HRID 1911497 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6344DichloromethaneHCID 662841-Heptanol, 7-bromo-HCID 86762179HCID 86762179, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-5a3cdb369ff64d53b4918e28170bd089
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604065B2

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