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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057219Generated: October 25, 2026

1,4-Dibromobutane → HCID 178485980, compound

https://huagongshe.com/reaction/2057219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178485979HCID 178485979—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
ProductHCID 178485980HCID 17848598031%

Reaction Steps

A solution of 11.6 g (containing 31 mmol) of crude trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester in 110 ml of 1,4-dibromobutane was treated with 3.16 g (9.3 mmol) tetrabutylammonium hydrogen sulfate and 200 ml of aqueous 50% NaOH and stirred for 2.5 days at RT. The reaction was extracted (CH2Cl2 2×). The organic phase was dried over Na2SO4, evaporated and purified by flash silica gel column (first with hexane to remove the dibromobutane and then hexane/EtOAc 1:1) to yield 4.06 g (31%) of trans-[4-(4-bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 3,4-difluoro-phenyl ester, MS: 420 (M, 1Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335687B2
Source datasetuspto-grants-2008_02
ORD IDord-e3f7741b58014254b3feeb4175979a45
Source noteuspto-grants-2008_02