HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544663Generated: November 1, 2026
Sodium hydride → 2-[4,5-Bis-(p-methoxyphenyl)-thiazol-2-ylthio]-2-formylacetic acid ethyl ester
https://huagongshe.com/reaction/544663
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4,5-Bis-(p-methoxyphenyl)-thiazoline-2-thione | HCID 13209656 | — |
| Reactant | 2-Bromoformylacetic acid ethyl ester | HCID 19802399 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 2-[4,5-Bis-(p-methoxyphenyl)-thiazol-2-ylthio]-2-formylacetic acid ethyl ester | HCID 54301956 | — |
Reaction Steps
3.3 g of 4,5-bis-(p-methoxyphenyl)-thiazoline-2-thione are dissolved in 50 ml of hexamethylphosphoric acid triamide, the solution is cooled to 5° and converted into the sodium salt under nitrogen with sodium hydride (0.5 g of a 50% strength suspension in mineral oil, de-oiled with hexane). The product is allowed to warm to room temperature, 2.0 g of 2-bromoformylacetic acid ethyl ester are added dropwise and the mixture is stirred at 25° for 1 hour, poured into 750 ml of ice-water and taken up in diethyl ether. The ethereal phase is washed with water, dried over magnesium sulphate and concentrated to dryness by evaporation. 2-[4,5-bis-(p-methoxyphenyl)-thiazol-2-ylthio]-2-formylacetic acid ethyl ester is obtained, which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04451471 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-6b038100b6d8430d896ce0aec8fc3af8 |
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| Source note | uspto-grants-1984_05 |
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