HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689176Generated: October 30, 2026
Ethanol → 7-(2-Chloroacetyl)-4-hydroxybenzo[d]thiazol-2(3H)-one
https://huagongshe.com/reaction/1689176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 7-Acetyl-4-hydroxybenzo[d]thiazol-2(3H)-one | HCID 45076987 | — |
| Reactant | Trimethylbenzylammonium Dichloroiodate | HCID 56924451 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-(2-Chloroacetyl)-4-hydroxybenzo[d]thiazol-2(3H)-one | HCID 57989327 | — |
Reaction Steps
Ethanol (1500 mL) was added to a mixture of 7-acetyl-4-hydroxy-3H-benzothiazol-2-one (150 g) (WO2004/016578) and benzyltrimethylammonium dichloroiodate (374 g) in a flask fitted with an overhead stirrer. The mixture was heated to 78° C. for 1 h and left to cool to room temperature overnight. The mixture was poured into water (2 L), and the precipitate collected by filtration, washed with water, filtered to near dryness, and suspended in ethyl acetate. The mixture was heated to reflux and allowed to cool to room temperature with stirring. The solid was collected by filtration, washed with cold ethyl acetate (200 mL) then re-suspended in diethyl ether (1 L). The solid was collected, filtered again and washed with ether (200 mL) and dried in vacuo to give the subtitled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148373B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-c4485b70703e43459770dbebccc7ab5d |
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| Source note | uspto-grants-2012_04 |
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