HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Succinimide → N-(2-cycloheptenyl)succinimide

HRID 1461582
Notes
Print preview

Reaction equation

HRID 1461582 reaction equation
Br[CH:2]1[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]=[CH:3]1.[C:9]1(=[O:15])[NH:13][C:12](=[O:14])[CH2:11][CH2:10]1.[Na].C1(=O)NC(=O)CC1.[H-].[Na+]>O.CN(C=O)C>[CH:2]1([N:13]2[C:9](=[O:15])[CH2:10][CH2:11][C:12]2=[O:14])[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]=[CH:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 11439SuccinimideHCID 24758Sodium hydrideHCID 124538813-Bromocyclohept-1-eneHCID 66769941Sodium succinimide

Product 1

HCID 13506505N-(2-cycloheptenyl)succinimide

Reagents, catalysts & solvents 2

HCID 962WaterSolvent
HCID 6228
Dimethylformamide
Solvent

Procedure

3-Bromocycloheptene (1.75 g) was added dropwise at room temperature to a DMF suspension (10 ml) of sodium succinimide prepared from succinimide (0.99 g) and 60% sodium hydride (0.40 g). This mixture was stirred at room temperature for 24 hours, poured into water (10 ml) and extracted with ether. The oily product obtained by concentration was purified by chromatography on silica gel to obtain 0.09 g of N-(2-cycloheptenyl)succinimide [Compound (214)].

Workup

  1. extractionextracted with ether
  2. customThe oily product obtained by concentration
  3. customwas purified by chromatography on silica gel

Sources & evidence

ORD record
ord-89b0334f9dac473ca34ed80919c6c267
Source dataset
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05075488

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes