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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190982Generated: October 30, 2026

Ammonium Chloride → Tert-butyl[6-(aminomethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate

https://huagongshe.com/reaction/2190982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl [6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetateHCID 66803873—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductTert-butyl[6-(aminomethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetateHCID 66803930—

Reaction Steps

Tert-butyl [6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-ylacetate] (1.98 g, 7.41 mmol) was dissolved in ethanol (20 mL) and water (10 mL). To the solution, iron powder (2.07 g, 37.0 mmol) and ammonium chloride (392.7 mg, 7.41 mmol) were added, and the mixture was stirred for 4.5 hours under heating to reflux. The mixture was allowed to cool, then diluted with saturated saline, a saturated aqueous solution of sodium bicarbonate, and ethyl acetate, and filtered through Celite to remove insoluble matter. The filtrate was separated into organic and aqueous layers. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a pale yellow solid (1.99 g, this compound was used directly in the next reaction without being purified).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324425B2
Source datasetuspto-grants-2012_12
ORD IDord-24fc45eb06c04a5ba70b612331699205
Source noteuspto-grants-2012_12