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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623056Generated: October 25, 2026

2-Bromophenylhydrazine hydrochloride → HCID 67238175, compound

https://huagongshe.com/reaction/1623056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromophenylhydrazine hydrochlorideHCID 2723912—
Reactanttert-Butyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylateHCID 2794767—
SolventAcetate-hydrochloric acidHCID 22641269—
ProductHCID 67238175HCID 67238175—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

A mixture of 2-bromophenylhydrazine hydrochloride (4.44 g, 19.81 mmol, Aldrich) and t-butyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate (4.48 g, 19.89 mmol, Chem-Impex) in 1 M HCl/acetic acid was stirred at 20-25° C. for 20 hours, and then heated at 65-70° C. for 48 hours. The mixture was cooled to room temperature and concentrated under vacuum. The residue was heated to boiling in absolute ethanol (25 mL) and the suspension was stirred at room temperature for 2 hours, then filtered. The solid was washed with cold ethanol and dried under vacuum to provide the title compound: 1H NMR (300 MHz, DMSO-d6) δ ppm 1.74-1.86 (m, 1H), 2.07 (t, J=9.7 Hz, 1H), 2.15-2.32 (m, 2H), 2.88 (d, J=17.4 Hz, 1H), 3.35-3.49 (m, 1H), 4.41 (s, 1H), 5.16 (d, J=4.4 Hz, 1H), 6.98 (t, J=7.7 Hz, 1H), 7.25-7.37 (m, 1H), 7.58 (d, J=7.9 Hz, 1H), 8.63-9.49 (m, 1H), 11.37 (s, 1H); MS (DCI/NH3) m/z 277/279 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778959B2
Source datasetuspto-grants-2014_07
ORD IDord-6cd066fcf4e444b78ea59c84c21acf22
Source noteuspto-grants-2014_07