Cyclohexyl bromide → HCID 67917236, compound

HRID 1534851Notes

Reaction equation

[CH2:1]([O:3][C:4]([C:6]1[CH:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2/[CH:18]=[C:19](/[C:21]([OH:23])=[O:22])\[CH3:20])[C:10]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[C:9]([CH3:29])[NH:8][C:7]=1[CH3:30])=[O:5])[CH3:2].[CH:31]1(Br)[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]1>>[CH2:1]([O:3][C:4]([C:6]1[CH:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2/[CH:18]=[C:19](\[CH3:20])/[C:21]([O:23][CH:31]2[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]2)=[O:22])[C:10]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[C:9]([CH3:29])[NH:8][C:7]=1[CH3:30])=[O:5])[CH3:2]

Participants

Reactant 2

HCID 7960Cyclohexyl bromide

HCID 67904952HCID 67904952, compound

Product 1

HCID 67917236HCID 67917236, compound

Procedure

From Compound A and cyclohexyl bromide stirring for 20 h at 40°.

Sources & evidence

ORD record: ord-3f422695ce9742e49b75eadf4e2fbcb9
Source dataset: uspto-grants-1992_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05091395

Reaction notes

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