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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219050Generated: October 31, 2026

6-Bromohexanenitrile → HCID 67147960, compound

https://huagongshe.com/reaction/2219050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-BromohexanenitrileHCID 81093—
ReactantHCID 87286888HCID 87286888—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 67147960HCID 67147960—

Reaction Steps

Tert-butyl-(benzyloxy)-(5-cyanopentyl)-carbamate (synthesized following the procedure described in EXAMPLE 1-Step 1a starting from 6-bromohexanenitrile) was dissolved in a saturated solution of HCl in EtOH and the mixture was stirred for 45 minutes. Nitrogen was bubbled into the solution to remove HCl in excess. The solvent was removed under reduced pressure and the residue, dissolved in 1,4-dioxane, was treated with triethylamine to adjust pH at 10. Ethanol was removed and the title compound containing an excess of triethylammonium chloride and ethyl 6-[(benzyloxy)amino]hexanoate was used without further purification. The analytical sample was purified by preparative RP-HPLC, using water (0.1% TFA) and acetonitrile (0.1% TFA) as eluents (column C18). The pooled product fractions were lyophilized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414045B2
Source datasetuspto-grants-2008_08
ORD IDord-91853f860afc49b9bf314a8601b9d26a
Source noteuspto-grants-2008_08