HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420723Generated: October 26, 2026
Hydrochloric Acid → (Z)-3-(2-hydroxaminoethyl)-5-fluoro-2-methyl-1-(4-methylthiobenzylidene)indene
https://huagongshe.com/reaction/1420723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Borane;pyridine | HCID 2723995 | — |
| Reactant | (Z)-5-Fluoro-2-methyl-1-(4-methylthiobenzylidene)-3-(2-hydroximinoethyl)indene | HCID 86745521 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (Z)-3-(2-hydroxaminoethyl)-5-fluoro-2-methyl-1-(4-methylthiobenzylidene)indene | HCID 86745522 | — |
Reaction Steps
To a suspension of the oxime from Step 3 (2.0 g, 5.9 mmol) in ethanol (35 mL) at 0° C. there was added pyridine-borane (1.1 g, 11.8 mmol) and 12 N aqueous HCl (1.48 mL, 17.75 mmol). The mixture was stirred at 0° C. for 1 hour, then warmed to room temperature. Most of the ethanol was evaporated, the residue was diluted with water and ethyl acetate (the product as hydrochloride salt remains in the organic phase) and was basified with 1N aqueous NaOH. The product obtained from the organic phase was triturated with hexane and was filtered to afford the title compound as a yellow solid, mp: 126° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06071934 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-c067d165c4074748bc1f5d6c587fdfbf |
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| Source note | uspto-grants-2000_06 |
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