HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265604Generated: October 30, 2026
Ethyl 2-chloroethanecarboximidate hydrochloride → HCID 69687596, compound
https://huagongshe.com/reaction/1265604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-chloroethanecarboximidate hydrochloride | HCID 12470659 | — |
| Reactant | HCID 86586796 | HCID 86586796 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69687596 | HCID 69687596 | 39.7% |
Reaction Steps
A mixture of 3-hydrazinothiocarbonyl-benzoic acid methyl ester trifluoroacetate (0.49 g) and 2-chloro-acetimidic acid ethyl ester hydrochloride (0.47 g) in EtOH (6 mL) was heated to 80° C. for 2.5 h. The mixture was diluted with AcOEt and washed with 1N HCl and with brine. The organic layer was dried and evaporated. The residual oil (0.8 g) was dissolved in MeOH (5 mL), MeONa (0.08 g) was added and the solution was heated to 65° C. for 0.5 h. The mixture was diluted with AcOEt and washed with 1N HCl and with brine. The organic layer was dried and evaporated and the residue was crystallized from AcOEt/hexane to give 3-(5-hydroxymethyl-[1,3,4]thiadiazol-2-yl) -benzoic acid methyl ester (0.15 g) as a white solid, MS (ISP) 251.2 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06544985B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-cb61eb6840f34fd2ad7c129baaf527e0 |
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| Source note | uspto-grants-2003_04 |
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