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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241627Generated: October 31, 2026

Ethoxalyl chloride → HCID 10215432, compound

https://huagongshe.com/reaction/1241627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
ReactantHCID 21936580HCID 21936580—
SolventDichloromethaneHCID 6344—
ProductHCID 10215432HCID 1021543264.3%

Reaction Steps

Ethyl chlorooxoacetate (0.46 mL, 4.10 mmol) was added to a stirring solution of the above thiourea (0.80 g, 2.74 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 0.61 g (64%) of 1-(4-tert-butyl-phenyl)-2-thioxo-3-(1,2,2-trimethyl-propyl)-imidazolidine-4,5-dione as a yellow solid: mp 208.9–209.5° C.; 1H NMR (DMSO-d6): δ 7.52 (d, 2H), 7.40 (d, 2H), 4.85 (q, 1H), 1.48 (d, 3H), 1.30 (s, 9H), 1.00 (s, 9H); IR (KBr): 3505, 2930, 1780 cm1; MS (m/z) 346 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115620B2
Source datasetuspto-grants-2006_10
ORD IDord-63be775197f34eabbfdb13cc8598ba9f
Source noteuspto-grants-2006_10