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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554564Generated: October 29, 2026

Methanol → (1R,2S,3R,6R)-6-[2-(4-Cyclopropyl-benzyl)phenoxy]-4-(hydroxymethyl)cyclohex-4-ene-1,2,3-triol

https://huagongshe.com/reaction/554564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPentamethylbenzeneHCID 12784—
ReactantBoron TrichlorideHCID 25135—
Reactant1-(4-Cyclopropylphenyl)methyl-2-[(1R,4R,5S,6S)-4,5,6-trisbenzyloxy-3-(benzyloxymethyl)-cyclohex-2-enyloxy]benzeneHCID 67461117—
SolventDichloromethaneHCID 6344—
Product(1R,2S,3R,6R)-6-[2-(4-Cyclopropyl-benzyl)phenoxy]-4-(hydroxymethyl)cyclohex-4-ene-1,2,3-triolHCID 1162513270%

Reaction Steps

In a nitrogen stream, a boron trichloride 1.0 M methylene chloride solution (160 μL, 0.16 mmol) was added to a solution of 1-(4-cyclopropylphenyl)methyl-2-[(1R,4R,5S,6S)-4,5,6-tris-benzyloxy-3-(benzyloxymethyl)-cyclohex-2-enyloxy]benzene (12 mg, 0.016 mmol) and pentamethylbenzene (24 mg, 0.17 mmol) in methylene chloride (300 μL) at −78° C., and the mixture was stirred at the same temperature for 1.5 hours. After addition of methanol, the temperature of the resulting solution was raised to room temperature and the solvent was distilled under reduced pressure. The obtained residue was purified by preparative TLC [developing solution=methanol:methylene chloride (1:8)] to obtain the title compound (4.1 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048897B2
Source datasetuspto-grants-2011_11
ORD IDord-1eaf7473534c44e092fd832a317b0749
Source noteuspto-grants-2011_11