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Ammonia → Ammonia

HRID 2051610
Notes
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Reaction equation

HRID 2051610 reaction equation
[NH3:1].[NH:2]1[CH2:6][CH2:5][CH2:4][C:3]1=[O:7].C(O)(=O)CCC(O)=[O:12]>O>[C:6]([CH2:5][CH2:4][C:3]([OH:7])=[O:12])#[N:2].[C:6]([CH2:5][CH2:4][C:3]([NH2:1])=[O:7])#[N:2].[NH:2]1[CH2:6][CH2:5][CH2:4][C:3]1=[O:7].[NH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 3

HCID 222AmmoniaHCID 1110Succinic AcidHCID 120252-Pyrrolidone2×

Product 4

HCID 222AmmoniaHCID 120252-PyrrolidoneHCID 2630863-Cyanopropanoic acidHCID 30172953-Cyanopropionamide

Reagents, catalysts & solvents 1

HCID 962WaterSolvent6×

Procedure

Preferably, the hydrogenation reaction is carried out in liquid phase with water being the liquid medium. The mol ratio of water to succinic reactant preferably is between 1:1 and 400:1, more preferably between 2:1 and 50:1 in the hydrogenation step reaction zone. Similar to the situation with ammonia, water may be added separately to the reaction zone if desired and also the amount of water in the reaction zone will be increased by the conversion of the succinic reactant to 2-pyrrolidone. In the case of conversion of succinic acid to 2-pyrrolidone, 3 mols of water are generated, and in the conversion of beta-cyanopropionic acid to 2-pyrrolidone, 1 mol of water will be formed, while in the conversion of beta-cyanopropionamide to 2-pyrrolidone, one mol of ammonia will be formed, but no water.

Workup

  1. customPreferably, the hydrogenation reaction

Sources & evidence

ORD record
ord-7f821d45c4ca4784bc63cc9acce36690
Source dataset
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04181662

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes