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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476956Generated: October 25, 2026

Ammonia → Cyclobutylmethylamine

https://huagongshe.com/reaction/476956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantCyclobutanecarbonyl chlorideHCID 78705—
ReactantCyclobutanecarboxamideHCID 1274476—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
ProductCyclobutylmethylamineHCID 409746—
ProductCyclobutanecarboxamideHCID 1274476—

Reaction Steps

(Aminomethyl)cyclobutane was prepared by lithium aluminum hydride reduction of cyclobutanecarboxamide according to the procedure of Shatkina, T. N.: Reutov, O. A., Dokl. Akad. Nauk. SSSR. (1975) 219:1148 [Chem. Abs. 82: 139453m]. Cyclobutanecarboxamide was prepared as follows: a solution of commercially available cyclobutanecarboxylic acid chloride (10 g) in ethyl ether (500 ml) was stirred at 0° while ammonia gas was introduced, resulting in a white precipitate. This material was collected by filtration and redissolved in 50 ml of ethanol/water (4:1, v/v). This solution was applied to a column containing 75 grams of AG 1-X8 ion exchange resin (hydroxide ion form) (obtained from Bio-Rad Company), and elution was continued with ethanol (1 liter). Evaporation of the eluate provided a quantitative yield (8.36 g) of cyclobutanecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886800
Source datasetuspto-grants-1989_12
ORD IDord-4cc0b2311df74178a0227e121489c24a
Source noteuspto-grants-1989_12