HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872538Generated: November 2, 2026
Dichloromethane → Ethyl 5-methoxythiazole-2-carboxylate
https://huagongshe.com/reaction/872538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Ethyl 2-(2-methoxy-2-oxoethylamino)-2-oxoacetate | HCID 3413524 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 5-methoxythiazole-2-carboxylate | HCID 67169140 | 7.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975254B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4263836c96bb4f2d8a4337928e947507 |
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| Source note | uspto-grants-2015_03 |
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