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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544896Generated: October 31, 2026

Water → 4-chloro-5-fluoro-1-(beta-D-glucopyranosyl)indoline

https://huagongshe.com/reaction/544896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
Reactant4-Chloro-5-fluoroindolineHCID 44182339—
SolventEthanolHCID 702—
Product4-chloro-5-fluoro-1-(beta-D-glucopyranosyl)indolineHCID 6719946794.2%

Reaction Steps

A mixture of 4-chloro-5-fluoroindoline (584 mg) and D-glucose (1.04 g) in ethyl alcohol (20 ml)-H2O (3 ml) was refluxed for 1.5 days. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform:methanol=100:0-85:15) to give 4-chloro-5-fluoro-1-(β-D-glucopyranosyl)indoline (1.07 g) as a colorless foam. APCI-Mass m/Z 334/336 (M+H). 1H-NMR (DMSO-d6) δ 3.02 (m, 3H), 3.20-3.45 (m, 4H), 3.57 (m, 2H), 3.71 (m, 1H), 4.35 (t, J=5.8 Hz, —H), 4.60 (d, J=8.3 Hz, 1H), 4.93 (d, J=5.1 Hz, 1H), 5.04 (d, J=4.0 Hz, 1H), 5.07 (d, J=4.3 Hz, 1H), 6.51 (dd, J=8.6, 3.6 Hz, 1H), 7.00 (t, J=9.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935674B2
Source datasetuspto-grants-2011_05
ORD IDord-db6ff6415a81482598da39d1dbfc0fb1
Source noteuspto-grants-2011_05