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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516253Generated: November 3, 2026

Methanol → HCID 57867352, compound

https://huagongshe.com/reaction/1516253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 57867350HCID 57867350—
SolventAmmoniaHCID 222—
ProductHCID 57867352HCID 5786735270%

Reaction Steps

(2R,3R,4R)-4-fluoro-2-(hydroxymethyl)-5-methoxy-4-methyl-tetrahydrofuran-3-yl benzoate (about 18 g, 63.3 mmol) in methanolic ammonia solution (25% w/w, 360 ml) was stirred at room temperature for about 36 hours, completion of the reaction monitored by thin-layer chromatography and methanol was removed under reduced pressure. Water added to the reaction mixture and extracted with ethyl acetate, the organic layer was dried over sodium sulphate and concentrated under reduced pressure. Purification by silica gel column chromatography using 20% ethyl acetate: hexane eluded the title compound (8 g) as an off-white solid. Yield: 70%; 1H NMR (300 MHz, CDCl3): δ 4.79 (d, 1H, J=10.8 Hz), 4.01-3.97 (m, 2H), 3.85 (d, 1H,), 3.71-3.66 (m, 1H), 3.44 (s, 3H), 2.05 (brs, 1H, —OH), 2.02 (brs, 1H, —OH), 1.47 (d, 3H, J=23.4 Hz); Mass: [M+Na]+: 203 (100%); IR cm−: 3437, 3372, 3294, 2924, 1459, 1102, 1049, 1006, 821, 731.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227431B2
Source datasetuspto-grants-2012_07
ORD IDord-be8a0612e03640ccb96f231ddfa1823d
Source noteuspto-grants-2012_07