HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065900Generated: October 26, 2026
Benzene → Ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate
https://huagongshe.com/reaction/1065900
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | HCID 178472904 | HCID 178472904 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate | HCID 73178131 | — |
Reaction Steps
A mixture of ethyl 2-hydroxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (22.0 g.), thioacetamide (7.5 g.) and benzene (100 ml.) was refluxed for 3 hours. After cooling triethylamine (10 g.) was added thereto and the mixture was stirred for 1 hour. An insoluble material was filtered off and the filtrate was concentrated under reduced pressure to give ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate (a mixture of syn and anti isomers) (8.6 g.). This substance was subjected to column chromatography on silica gel (80 g.) using benzene as developing solvent. Firstly the eluate containing anti isomer was eluted, collected and concentrated to give ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate (anti isomer) (2.5 g.), mp 90° to 92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04331664 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-0b31455c4fdf4484ba7d6c496b034ca8 |
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| Source note | uspto-grants-1982_05 |
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