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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966143Generated: November 1, 2026

Methanol → Methyl 3-oxocyclobutane-1-carboxylate

https://huagongshe.com/reaction/1966143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3-Oxocyclobutane-1-carboxylic acidHCID 4913358—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductMethyl 3-oxocyclobutane-1-carboxylateHCID 1399236780.64%

Reaction Steps

A solution of N,N′-dicyclohexylcarbodiimide (7.17 g, 0.0347 mol) in methylene chloride (8 mL, 0.1 mol) was added dropwise to a stirred mixture of 3-oxocyclobutanecarboxylic acid (3.6 g, 0.032 mol), methanol (2.6 mL, 0.063 mol) and 4-dimethylaminopyridine (3.08 g, 0.0252 mol) in methylene chloride (20 mL, 0.2 mol). The mixture was stirred at rt for 24 h, then filtered through Celite. The filtrate was washed with 0.5 M HCl and sat. sodium bicarbonate, dried and concentrated to dry. The residue was purified on silica gel, eluting with 0 to 40% EtOAc in hexane, to give the desired ester (3.26 g, 80.64%). 1H NMR (CDCl3, 400 MHz): 3.78 (s, 3H), 3.43˜3.20 (5H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-c2d79128c70a405b9b58200327575b05
Source noteuspto-grants-2013_04