Bromomethylstyrene → HCID 18412163, compound

HRID 992367Notes

Reaction equation

HRID 992367 reaction equation
[O:1]([C:8]1[CH:13]=[CH:12][C:11]([CH:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:20](Br)[CH:21]=[CH:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[O:1]([C:8]1[CH:13]=[CH:12][C:11]([CH:14]2[CH2:19][CH2:18][N:17]([CH2:20]/[CH:21]=[CH:22]/[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH2:16][CH2:15]2)=[CH:10][CH:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 98116BromomethylstyreneHCID 110759844-(4-Phenoxyphenyl)piperidine

Product 1

HCID 18412163HCID 18412163, compound

Procedure

The same procedure was followed as in Example 11 using the compound (9) synthesized in Example 2 and cinnamyl bromide to produce the above.

Workup

  1. customto produce the above

Sources & evidence

ORD record
ord-7ac95d70ac804dae8967325719e2af14
Source dataset
uspto-grants-2002_10
Patent number
US06469010B1

Reaction notes

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