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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672418Generated: November 2, 2026

Sodium borohydride → HCID 59759989, compound

https://huagongshe.com/reaction/1672418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67313482HCID 67313482—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 59759989HCID 5975998978.9%

Reaction Steps

To a solution of 80 mg (0.19 mmol) of 5-(2-chlorophenyl)-3-(2,4-dichlorophenyl)-4-[(3-pyridyl)carbonyl]isoxazole in 3 mL of ethanol at 0° C. was added 40 mg (1.06 mmol) of sodium borohydride. The mixture was stirred for 2 hrs and then diluted with ethyl acetate. The ethyl acetate solution was washed with saturated sodium chloride solution and dried over magnesium sulfate. The drying agent was filtered off, and the ethyl acetate was removed by rotoevaporation. The crude product was purified by prep TLC to give 65 mg (0.15 mmol) of 5-(2-chlorophenyl)-3-(2,4-dichlorophenyl)-4-[(3-pyridyl)hydroxymethyl]-isoxazole. 1H NMR (CDCl3): δ 5.80 (br s, 1), 6.97 (m,1), 8.23 (br s, 1), and 8.28 ppm (br s, 1). MS m/z: 431.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998983B2
Source datasetuspto-grants-2011_08
ORD IDord-606757f6196240da91cfed66afc2c309
Source noteuspto-grants-2011_08