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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417714Generated: November 3, 2026

Methanol → 4-(6-Chloro-1,2-benzisoxazol-3-yl)-1-piperidinecarboxaldehyde

https://huagongshe.com/reaction/2417714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86738605HCID 86738605—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-(6-Chloro-1,2-benzisoxazol-3-yl)-1-piperidinecarboxaldehydeHCID 1307642180.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469869
Source datasetuspto-grants-1984_09
ORD IDord-5718845c1b1e4d39bb4041904aa5ba5c
Source noteuspto-grants-1984_09