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Hydrogen Bromide → L-Proline ethylamide

HRID 1583721
Notes
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Reaction equation

HRID 1583721 reaction equation
Br.[CH2:2]([NH:4][C:5](=[O:21])[C@@H:6]1[CH2:10][CH2:9][CH2:8][N:7]1C(OCC1C=CC=CC=1)=O)[CH3:3].CCOCC>C(O)(=O)C>[CH2:2]([NH:4][C:5](=[O:21])[C@@H:6]1[CH2:10][CH2:9][CH2:8][NH:7]1)[CH3:3]
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 260Hydrogen BromideHCID 3283Diethyl EtherHCID 685185(S)-Benzyl 2-(ethylcarbamoyl)pyrrolidine-1-carboxylate

Product 1

HCID 7408609L-Proline ethylamide

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent2×

Procedure

40 ml. of 36% hydrogen bromide in acetic acid was added to 11 grams of a solution of benzyloxycarbonyl proline ethylamide in 10 ml. of acetic acid. After 1 hour 300 ml. of ether was added to the reaction solution, so resulting in the separation of a non-crystalline hydrobromide. The hydrobromide was dried for 2 hours in desiccator over phosphorus pentoxide and sodium hydroxide, and then suspended in 60 ml. of a saturated amoniacal solution of chloroform at 0 degrees C. The resultant suspension was permitted to stand at 3 degrees C. for 20 minutes and then filtered, the filtrate being evaporated. 5.7 g of a non-crystalline product was obtained. Rf 0.25/S1 ; 0.56/S2.

Sources & evidence

ORD record
ord-d8526e07b21a44a183d7a89cc7c4e73c
Source dataset
uspto-grants-1985_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04554100

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes