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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872538Generated: November 2, 2026

Dichloromethane → Ethyl 5-methoxythiazole-2-carboxylate

https://huagongshe.com/reaction/872538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantEthyl 2-(2-methoxy-2-oxoethylamino)-2-oxoacetateHCID 3413524—
SolventChloroformHCID 6212—
ProductEthyl 5-methoxythiazole-2-carboxylateHCID 671691407.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 2-(2-methoxy-2-oxoethylamino)-2-oxoacetate (1.00 g, 5.29 mmol) and phosphorus pentasulfide (1.29 g, 5.82 mmol) in chloroform (20 ml) was stirred at 60° C. for 7 h. To the cooled reaction mixture DCM (100 ml) was added and the mixture was washed with water (50 ml) and brine (50 ml). Organic phase was dried over Na2SO4 and evaporated. Evaporation residual was dissolved in dry MeCN (10 ml) and phosphorus pentoxide (0.75 g, 5.29 mml) was added and the mixture was heated to reflux for 4.5 h. To the cooled reaction mixture water (35 ml) was added and the mixture was extracted with EtOAc (3×50 ml). Combined organic fractions were dried over Na2SO4 and evaporated to give crude product, which was purified twice by CombiFlash (1st column: silica, eluent: 0-100% EtOAc in heptane; 2nd column: C-18, eluent: 0-100% MeCN in water) to yield 73 mg (7%) of the title compound. 1H-NMR (400 MHz; CDCl3): δ 1.42 (t, 3H), 4.01 (s, 3H), 4.43 (q, 2H), 7.30 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975254B2
Source datasetuspto-grants-2015_03
ORD IDord-4263836c96bb4f2d8a4337928e947507
Source noteuspto-grants-2015_03