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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748162Generated: October 30, 2026

Methanol → HCID 67983676, compound

https://huagongshe.com/reaction/1748162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 67984108HCID 67984108—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67983676HCID 67983676—

Reaction Conditions

Temperature0 °C

Reaction Steps

(5-cyclopropyl-3-2-phenylcyclopropyl)isoxazol-4-yl)methanol (rac-I-6F). To a solution of 5-cyclopropyl-3-(2-phenylcyclopropyl)isoxazole-4-carboxylic acid rac-I-6E (0.49 g, 1.82 mmol) in THF and cooled to 0°C. lithium aluminum hydride (4.5 mL, of a 1M solution in THF) was added dropwise. After stirring fo(12 h at rt, the reaction mixture was cooled back to 0°C. and quenched by dropwise addition of H2O (0.5 mL), 15% NaOH (0.5 mL), H2O (1 mL) followed by Na2SO4 and filtered through CELITE® under vacuum. The crude was purified by column chromatography on silica gel with DCM-EtOAc 0 to 5% gradient as eluent to give (5-cyclopropyl-3-(2-phenylcyclopropyl)isoxazol-4-yl)methanol. 1H NMR (400 MHz, DMSO) δ 7.31-727 (m, 2H), 7.21-7.17 (m, 3H), 5.00 (t, J=5.2 Hz, 1H), 4.42-4.33 (m, 2H), 2.39-2.35 (m, 1H), 2.23-2.13 (m, 2H), 1.57-1.52 (m, 1H), 1.46-1.42 (m, 1H), 1.05-1.04 (m, 2H), 0.95-0.91 (M, 2H). MS m/z 256.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150568B2
Source datasetuspto-grants-2015_10
ORD IDord-0b926365ac8343989cd9ee378078093e
Source noteuspto-grants-2015_10