HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219050Generated: October 31, 2026
6-Bromohexanenitrile → HCID 67147960, compound
https://huagongshe.com/reaction/2219050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Bromohexanenitrile | HCID 81093 | — |
| Reactant | HCID 87286888 | HCID 87286888 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67147960 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414045B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-91853f860afc49b9bf314a8601b9d26a |
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| Source note | uspto-grants-2008_08 |
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