HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223570Generated: October 30, 2026
Methanol → 4-(6-Chloro-1,2-benzisoxazol-3-yl)-1-piperidinecarboxaldehyde
https://huagongshe.com/reaction/223570
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86738605 | HCID 86738605 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(6-Chloro-1,2-benzisoxazol-3-yl)-1-piperidinecarboxaldehyde | HCID 13076421 | 80.8% |
Reaction Steps
To a stirred suspension of 1.25 g of sodium hydride (prepared from 2.5 g 50% oil dispersion) in 100 ml of tetrahydrofuran was added, over 20 mins, a solution of 10 g of 1-formyl-4-(2,4-dichlorobenzoyl)piperidine O-formyl oxime in 60 ml of dimethylformamide and 40 ml of tetrahydrofuran. The stirred mixture was heated to 80°-90° (oil bath temperature) for 5 hrs and after standing at 20° for 16 hrs, 10 ml of methanol and 20 ml of water were added. The reaction mixture was added to about 1.2 l of saturated sodium chloride solution. The mixture was extracted with 400 ml of ether. The extract was washed with 800 ml of water. The aqueous phase was extracted with 400 ml of ether and the combined ether extracts were distilled to yield an oil, which crystallized on standing. Recrystallization from isopropanol-ether gave 6.5 g (67.2%) of product, mp, 114°- 115°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04355037 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-2d86fbeb6699474e920dc07517e82160 |
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| Source note | uspto-grants-1982_10 |
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