Hydrochloric Acid → 4-(5-Methoxy-1-naphthalenyloxy)piperidine hydrochloride

HRID 325960Notes

Reaction equation

HRID 325960 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[C:8]2[O:13][CH:14]1[CH2:19][CH2:18][N:17](C(OC=C)=O)[CH2:16][CH2:15]1.[ClH:25]>CO>[ClH:25].[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[C:8]2[O:13][CH:14]1[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 204632014-(5-Methoxy-1-naphthalenyloxy)-1-(vinyloxycarbonyl)piperidine

Product 1

HCID 204632304-(5-Methoxy-1-naphthalenyloxy)piperidine hydrochloride

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

The thus obtained 4-(5-methoxy-1-naphthalenyloxy)-1-(vinyloxycarbonyl)piperidine is stirred for 2 hours with 2 N HCl in methanol to yield 4-(5-methoxy-1-naphthalenyloxy)piperidine hydrochloride.

Sources & evidence

ORD record
ord-acad4ac362644af0bad99b7e286255af
Source dataset
uspto-grants-1984_04
Patent number
US04443462

Reaction notes

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