HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543892Generated: October 31, 2026
(2-thioxo-1,3-benzothiazol-3(2H)-yl)acetic acid → Methyl (2-sulfanylidene-1,3-benzothiazol-3(2H)-yl)acetate
https://huagongshe.com/reaction/543892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2-thioxo-1,3-benzothiazol-3(2H)-yl)acetic acid | HCID 351524 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl (2-sulfanylidene-1,3-benzothiazol-3(2H)-yl)acetate | HCID 13034583 | 94% |
Reaction Steps
To a stirred solution containing 45.1 g (0.2 mol) of 3-(carboxymethyl) benzothiazoline-2-thione in 600 ml of methyl alcohol, 142.0 g (1.0 mol) of boron trifluoride ether complex was added in one portion. An exothermic reaction set in causing a temperature rise from 20° to 37° C. The stirred solution was heated at reflux for 24 hours and then cooled to 0° C. After cooling, 1400 ml of 10% aqueous sodium bicarbonate was slowly added (foaming observed) at 0°-10° C. until pH 8 was obtained. After stirring at 0°-10° C. for one hour, the solid was collected by filtration, washed with water until neutral to litmus and air-dried at 25°-30° C. The product, 2-thioxo-3(2H)-benzothiazoleacetic acid, methyl ester was obtained in 94% yield, m.p. 127°-128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04447618 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-8fd6b2cec0644f53ba68ebf61a3cf82f |
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| Source note | uspto-grants-1984_05 |
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