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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355194Generated: October 29, 2026

Propanoic acid, 2-bromo-2-methyl-, ethyl ester → 4695-19-6

https://huagongshe.com/reaction/355194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
Product4695-19-6HCID 137701547—

Reaction Steps

A suspension of thiourea (19.0 g, 0.25 mole) in 150 ml of ethanol was heated under reflux until all of the thiourea had dissolved. Ethyl 2-bromo-isobutyrate (49.0 g, 0.25 mole) was then added over 10 minutes to the refluxing solution, after which time the solution was heated under reflux for six hours then allowed to stir at ambient temperature 36 hours. The solution was concentrated to dryness and the residue treated with water, then with aqueous NaHCO3 to adjust the pH to 7.0. The precipitated solid was collected by filtration, washed with water and dried to yield 5,5-dimethyl-2-iminothiazolidin-4-one: mp 252°-254° C.; 15.0 g (0.12 mole, 47%). Structure was confirmed by IR and NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04378357
Source datasetuspto-grants-1983_03
ORD IDord-80212aeb42cb417da650a65c5c639c4b
Source noteuspto-grants-1983_03