HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049278Generated: November 3, 2026
Sodium Bicarbonate → HCID 54074940, compound
https://huagongshe.com/reaction/2049278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | HCID 53841316 | HCID 53841316 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54074940 | HCID 54074940 | 52.7% |
Reaction Steps
In 350 ml of tetrahydrofuran is dissolved 52 g of methyl 4-bromo-3-oxo-2-methoxyiminobutyrate, followed by addition of 250 ml of water. Then, 89.1 g of sodium acetate trihydrate and 33.2 g of thiourea are added and the mixture is reacted with stirring at room temperature for 18 hours. To this reaction mixture is added 200 ml of a 5% aqueous solution of sodium hydrogen carbonate and the mixture is extracted with ethyl acetate. The organic layer is washed with water, dried and distilled under reduced pressure to remove the solvent. To the residue is added 200 ml of ether and the resultant crystals are collected by filtration. By the above procedure is obtained 24.8 g of methyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetate (syn-isomer) as crystals melting at 164.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04197298 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-c911d4351b3140698eb92cd93ad515b3 |
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| Source note | uspto-grants-1980_04 |
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