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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241618Generated: October 31, 2026

Ethoxalyl chloride → HCID 10126274, compound

https://huagongshe.com/reaction/1241618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
ReactantHCID 21936576HCID 21936576—
SolventDichloromethaneHCID 6344—
ProductHCID 10126274HCID 1012627479%

Reaction Steps

Ethyl chlorooxoacetate (0.496 mL, 4.44 mmol) was added to a stirring solution of the above thiourea (0.70 g, 2.22 mmol) in dichloromethane (15 mL) and the resulting mixture was stirred overnight at room temperature. Concentration, trituration of the residue with diethyl ether, and recrystallization from boiling methanol afforded 0.647 g (79%) of 1-(4-bromo-phenyl)-2-thioxo-3-(1,2,2-trimethyl-propyl)-imidazolidine-4,5-dione as a yellow solid: mp 207.1–207.9° C.; 1H NMR (DMSO-d6): δ 7.74 (d, 1H), 7.32 (d, 2H), 4.81 (q, 1H), 1.48 (d, 3H), 0.99 (s, 9H); IR (KBr): 3500, 2970, 2230, 1770, 1500 cm−1; MS (m/z) 368 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115620B2
Source datasetuspto-grants-2006_10
ORD IDord-cb756d3b72154454b40b610c921cb407
Source noteuspto-grants-2006_10