1-Bromo-2-(methoxymethyl)naphthalene → HCID 22451510, compound

HRID 2185643Notes

Reaction equation

HRID 2185643 reaction equation
[ClH:1].[C:2]1([CH:8]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[N:9]2[CH2:12][CH:11]([O:13][C:14]3[C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH:17]=[CH:16][C:15]=3COC)[CH2:10]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.BrC1C2C(=CC=CC=2)C=CC=1[CH2:44][O:45]C>>[ClH:1].[C:27]1([CH:8]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[N:9]2[CH2:10][CH:11]([O:13][C:14]3[C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH:17]=[CH:16][C:15]=3[O:45][CH3:44])[CH2:12]2)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

Participants

3

Reactant 2

HCID 123857651-Bromo-2-(methoxymethyl)naphthaleneHCID 22451516HCID 22451516, compound

Product 1

HCID 22451510HCID 22451510, compound

Procedure

1-(Diphenylmethyl)-3-[(2-(methoxymethyl)-1-naphthalenyl)oxy]-azetidine hydrochloride, M.S. (C.I.) (M/Z): 410 [M+H]+, starting from 1-bromo-2-(methoxymethyl)-naphthalene.

Sources & evidence

ORD record
ord-02ca87b4d6bc440c8680b5047d0384a6
Source dataset
uspto-grants-2002_06
Patent number
US06403573B1

Reaction notes

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