Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855401Generated: October 31, 2026

Sodium Hydroxide → HCID 178433444, compound

https://huagongshe.com/reaction/1855401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68630388HCID 68630388—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178433444HCID 17843344475.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of acetamidine hydrochloride (0.617 g, 6.53 mmol) in methanol (10 mL) was added potassium tert.-butoxide (0.80 g, 6.54 mmol) followed by methyl 3-[1-(4-chlorophenyl)cyclobutyl]-3-oxopropionate (1.34 g, 5.02 mmol). The mixture was stirred at 20° C. for 16 h, then refluxed for 2 h. The reaction mixture was cooled, diluted with water, made alkaline by the addition of 10 mL of 10% aqueous sodium hydroxide solution, and then washed with diethyl ether. The aqueous phase was acidified with concentrated hydrochloric acid, and then extracted with diethyl ether. This ether extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure to give the title compound (1.04 g, 75%) as a solid foam. Mp 130-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-79a6dfa51d9243b9b73c27f7bedd0f3a
Source noteuspto-grants-2015_02