HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385116Generated: October 30, 2026
Formaldehyde → 3-(4-Benzyloxy-3-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole
https://huagongshe.com/reaction/385116
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Benzothiazoline | HCID 96588 | — |
| Reactant | 4-Benzyloxy-3-trifluoromethylbenzoyl chloride | HCID 86668175 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-(4-Benzyloxy-3-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole | HCID 68108976 | — |
Reaction Steps
2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (282 mg) and 37% formalin (0.19 mL) in the same manner as in Example 1 was dissolved in chloroform (6 mL), and triethylamine (0.62 mL) and 4-benzyloxy-3-trifluoromethylbenzoyl chloride were added to the solution, and then the mixture was stirred at mom temperature for 1.5 hours. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1) to obtain the title compound (356 mg) as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367843B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-20241d3e0d9f4098ac481fe66ad2b1ea |
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| Source note | uspto-grants-2013_02 |
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