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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689801Generated: November 1, 2026

Methanol → (5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanol

https://huagongshe.com/reaction/1689801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTolueneHCID 1140—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole-4-carboxylateHCID 53421832—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanolHCID 4579038285.5%

Reaction Steps

Diisobutylaluminium hydride 1M/toluene (4.62 L, 4.62 mol) is added dropwise to a stirred solution of 5-Cyclopropyl-3-(2,6-dichloro-phenyl)-isoxazole-4-carboxylic acid methyl ester (687.14 g, 2.20 mol) in THF (4.4 L) at 0° C. The reaction is stirred at room temperature for 2 hours. Methanol (150 mL) is added over the mixture at 0° C. and stirred for 10 min. Then, water (2.2 L) and EtOAc (4.3 L) is added. The precipitate formed is filtered through celite and all the solvents are removed in vacuum. The solid is triturated in 1 L of hexane and dried under vacuum filtration to obtain title compound (534.7 g, 85% yield) as a white solid. MS (m/e): 312 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153624B2
Source datasetuspto-grants-2012_04
ORD IDord-6861bdfa0f9040e58431e71ada8b07bc
Source noteuspto-grants-2012_04