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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303919Generated: November 1, 2026

1-Bromohexane → HCID 18537656, compound

https://huagongshe.com/reaction/2303919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantSodium hydrideHCID 24758—
ReactantHCID 69820608HCID 69820608—
SolventDimethylformamideHCID 6228—
ProductHCID 18537656HCID 18537656168.8%

Reaction Steps

To a suspension of sodium hydride (55 wt. %, 1.26 g) in anhydrous N,N-dimethylformamide (100 ml) was added N-[5-(4-t-butoxycarbonylaminophenoxy)-2-nitrophenyl]-N-methylcarbamate (12.1 g). The mixture was stirred at ambient temperature for several minutes. To the mixture was added hexyl bromide (6.5 g) under ice cooling and the mixture was stirred at the same temperature for 30 minutes and then at room temperature for 1.0 hour. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by chromatography on a silica gel column using toluene/diisopropyl ether=100/7 as the eluant to give the title compound (13.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432993B1
Source datasetuspto-grants-2002_08
ORD IDord-adc5012f85c64e84b4f320e6ceb51ee5
Source noteuspto-grants-2002_08