HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834796Generated: October 31, 2026
2-Mercaptoethanol → HCID 178472918, compound
https://huagongshe.com/reaction/1834796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178472915 | HCID 178472915 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178472918 | HCID 178472918 | — |
Reaction Steps
Ethyl 4-chloro-2-hydroxyimino-3-oxo-butyrate (340 g.) is dissolved in chloroform (1.5 liters) and 2-mercapto-ethanol (126 cc.) is then added. Triethylamine (248 cc.) dissolved in chloroform (1 liter) is added to the resulting solution at about 20° C., over the course of 30 minutes. The reagents are left in contact for 15 hours whilst stirring at about 20° C. Then the reaction mixture is washed with water (200 cc.) followed by 2 N hydrochloric acid (200 cc.) and finally four times with water (a total of 1 liter). The organic phase is dried over sodium sulphate treated with decolourising charcoal, filtered and concentrated to dryness under reduced pressure (20 mm.Hg). Ethyl 4-(2-hydroxy-ethylthio)-2-hydroxyimino-3-oxo-butyrate (321 g.) is thus obtained in the form of an oil which gradually solidifies.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04071531 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-176d1402f0934ddd8a5419367dc68c22 |
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| Source note | uspto-grants-1978_01 |
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