Hydrochloric Acid → HCID 70206818, compound

HRID 443241Notes

Reaction equation

HRID 443241 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][C@@H:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([CH3:20])[CH:15]=2)[C@H:10]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:9]1)=O)(C)(C)C.[ClH:29]>CCOC(C)=O>[ClH:29].[CH3:20][C:16]1[CH:15]=[C:14]([C@@H:11]2[CH2:12][CH2:13][NH:8][CH2:9][C@H:10]2[O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:19]=[CH:18][CH:17]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 70244349HCID 70244349, compound

Product 1

HCID 70206818HCID 70206818, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

To a solution of trans-N-t butoxycarbonyl-4-(3-methylphenyl)-3-benzyloxy piperidine, (0.137 g, 3.60 mmol) in EtOAc (50 ml) at 0° C. was bubbled HCl gas until saturated. The reaction was strirred at 0° C. for 10 min and then the solvent evaporated in vacuo to afford the product as a white foam.

Workup

  1. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-00a2006afd5c4585af21398f41c1a23d
Source dataset
uspto-grants-1999_04
Patent number
US05891889

Reaction notes

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