Phenethyl bromide → HCID 23396189, compound

HRID 491451Notes

Reaction equation

BrCCC1C=CC=CC=1.[ClH:10].[CH3:11][O:12][C:13]1[CH:14]=[C:15]([C:21]2[C@@H:30]3[C@@H:25]([CH2:26][CH:27]=[CH:28][CH2:29]3)[C:24](=[O:31])[N:23]([CH:32]3[CH2:37][CH2:36][N:35]([CH2:38][C:39]4[CH:48]=[C:47]5[C:42]([CH:43]=[CH:44][C:45](=O)O5)=CC=4)[CH2:34][CH2:33]3)[N:22]=2)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]>>[ClH:10].[CH3:11][O:12][C:13]1[CH:14]=[C:15]([C:21]2[C@@H:30]3[C@@H:25]([CH2:26][CH:27]=[CH:28][CH2:29]3)[C:24](=[O:31])[N:23]([CH:32]3[CH2:33][CH2:34][N:35]([CH2:38][CH2:39][C:48]4[CH:47]=[CH:42][CH:43]=[CH:44][CH:45]=4)[CH2:36][CH2:37]3)[N:22]=2)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]

Participants

Reactant 2

HCID 7666Phenethyl bromide

HCID 86601097HCID 86601097, compound

Product 1

HCID 23396189HCID 23396189, compound

Procedure

Prepared from 2-bromoethylbenzene and starting compound A1 as described for compound 18. M.p. 216-217° C.

Sources & evidence

ORD record: ord-63f20ab3255d4195a09dbe2d4c24efd9
Source dataset: uspto-grants-2009_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07531540B2

Reaction notes

Loading…