HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704938Generated: October 31, 2026
Hydrochloric Acid → Ethyl 2-(2-tritylamino-4-thiazolyl)-2-ethoxyiminoacetate
https://huagongshe.com/reaction/704938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | HCID 53897917 | HCID 53897917 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 2-(2-tritylamino-4-thiazolyl)-2-ethoxyiminoacetate | HCID 54531085 | 125.1% |
Reaction Steps
3.98 g of trityl chloride were slowly added under an inert atmosphere to a mixture of 3.16 g of the product of Step A, 6 ml of dimethylformamide, 12 ml of methylene chloride and 1.89 ml of triethylamine cooled to -15° C. and the mixture stood at 10° C. for 30 minutes and then 3 hours at room temperature. 13 ml of N hydrochloric acid were added to the mixture which was stirred and decanted. The organic phase was washed with N hydrochloric acid, then with water and was extracted with methylene chloride. The extracts were dried and evaporated to dryness to obtain 7.89 g of raw ethyl 2-(2-tritylamino-4 -thiazolyl)-2-ethoxyiminoacetate having a syn configuration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988816 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-ee2a6d54a94a4329a02b015b3025a196 |
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| Source note | uspto-grants-1991_01 |
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