1,5-Dibromopentane → HCID 178485972, compound

HRID 25546Notes

Reaction equation

HRID 25546 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9](=[O:19])[N:10]([C@H:12]2[CH2:17][CH2:16][C@H:15]([OH:18])[CH2:14][CH2:13]2)[CH3:11])=[CH:4][CH:3]=1.[Br:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]Br>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][C:9](=[O:19])[N:10]([C@H:12]2[CH2:17][CH2:16][C@H:15]([O:18][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][Br:20])[CH2:14][CH2:13]2)[CH3:11])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 81001,5-DibromopentaneHCID 178485970HCID 178485970, compound

Product 1

HCID 178485972HCID 178485972, compound

Procedure

In analogy to example 11.5, trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester and 1,5-dibromopentane were reacted to yield trans-[4-(5-Bromo-pentyloxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester as yellow oil, MS: 433 (MH+, 1Br, 1Cl).

Sources & evidence

ORD record
ord-664aa3c04c5a4769afcb66fc186f71c0
Source dataset
uspto-grants-2005_02
Patent number
US06858651B2

Reaction notes

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