Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514207Generated: November 4, 2026

Hydroxyamine hydrochloride → HCID 178451593, compound

https://huagongshe.com/reaction/1514207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 7-cyano-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylateHCID 18173275—
SolventEthanolHCID 702—
ProductHCID 178451593HCID 17845159393%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 1,1-dimethylethyl 7-cyano-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate (may be prepared as described in WO2002040471) (5 g, 18.36 mmol), hydroxylamine hydrochloride (2.55 g, 36.7 mmol) and sodium bicarbonate (7.71 g, 92 mmol) in ethanol (250 ml) was heated at 50° C. overnight. Further hydroxylamine hydrochloride (0.638 g, 9.18 mmol) was added to the reaction mixture and heating at 50° C. continued for 5 h. The reaction mixture was allowed to cool and the solid filtered off, the solution was concentrated in vacuo to yield the title compound as a white solid (5.77 g, 17.01 mmol, 93% yield). δH (d6DMSO, 400 MHz): 9.56 (1H, s), 7.52-7.37 (2H, m), 7.14 (1H, d), 5.77 (2H, br s), 3.50-3.32 (4H, m), 2.91-2.80 (4H, m), 1.41 (9H, s). MS (ES): C16H23N3O3 requires 305; found 306 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222245B2
Source datasetuspto-grants-2012_07
ORD IDord-fec3b730e37d487dbeacced12eb81940
Source noteuspto-grants-2012_07