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Morpholine → 12-Morpholinyldodecylphthalimide

HRID 1463810
Notes
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Reaction equation

HRID 1463810 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]1[CH:24]=[CH:23][CH:22]=[C:16]2[C:17]([NH:19][C:20](=[O:21])[C:15]=12)=[O:18].[NH:25]1[CH2:30][CH2:29][O:28][CH2:27][CH2:26]1>C(OCC)C>[N:25]1([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]2[CH:24]=[CH:23][CH:22]=[C:16]3[C:17]([NH:19][C:20](=[O:21])[C:15]=23)=[O:18])[CH2:30][CH2:29][O:28][CH2:27][CH2:26]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 8083MorpholineHCID 1993351212-Bromododecylphthalimide

Product 1

HCID 5450314412-Morpholinyldodecylphthalimide

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

12-Bromododecylphthalimide (623 mg; 2.0 mmoles) and morpholine (0.35 ml; 4.0 mmoles) were dissolved in anhydrous ethyl ether (5 ml). Reaction times and process as per Example 1.

Workup

  1. customReaction times and process as per Example 1

Sources & evidence

ORD record
ord-b31fe77b8bf04b1785730aa9d24fbd2d
Source dataset
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05302593

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes