HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073696Generated: October 31, 2026
Carbon Disulfide → Methyl 5-(benzylsulfanyl)-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/2073696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-(benzylsulfanyl)-1,3-thiazole-4-carboxylate | HCID 15077124 | — |
Reaction Steps
A solution of 31.3 g of potassium t-butoxide in 280 ml of tetrahydrofuran was cooled to -50° and a solution of 27.7 g of methyl isocyanoacetate in 230 ml of tetrahydrofuran was addd dropwise at -50° to -40°. The resulting brown suspension was stirred 15 minutes then cooled to -78°, then a solution of 16.8 ml of carbon disulfide in 225 ml tetrahydrofuran was added dropwise while maintaining the temperature below -50°. The pinkish-brown thick suspension was allowed to warm to -15° to 10° over 15 to 20 minutes. To the reaction mixture, a solution of 33.3 ml of benzyl bromide in 140 ml tetrahydrofuran was added dropwise at -15° to -5°. The reaction mixture was stirred at ambient temperature for 30 minutes, refluxed for 20 minutes, then cooled and the bulk of the solvent evaporated. To the oily residue, 1000 ml ice-water was added. After several minutes, the product solidified. The tan solid was collected, washed twice with water, followed by hexane and dried giving 68.8 g of methyl 5-(phenylmethylthio)-4-thiazolecarboxylate, m.p. 90°-92°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04919706 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-c7cd5f3fcfe74dc3ad0581d516a7758b |
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| Source note | uspto-grants-1990_04 |
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