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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944100Generated: November 2, 2026

4-Toluenesulfonyl chloride → HCID 86668483, compound

https://huagongshe.com/reaction/1944100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 52914724HCID 52914724—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 86668483HCID 86668483319.9%

Reaction Steps

To a stirred solution of {(3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-2-hydroxymethyl-tetrahydro-pyran-2-yl}-methanol (Example 9, 500 mg, 0.70 mmol) in pyridine (15 mL) was added p-toluene sulfonyl chloride (670 mg, 0.21 mmol). After stirring for overnight at room temperature, reaction mixture was heated to 80° C. for another 18 h. The volatiles were evaporated, resulting residue was taken in ethyl acetate and washed with 1N HCl, brine, concentrated to furnish toluene-4-sulfonic acid (3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-2-hydroxymethyl-tetrahydro-pyran-2-ylmethyl ester (580 mg). The crude product was used as such for next step without purification which also contains small amount of bis-tosylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394772B2
Source datasetuspto-grants-2013_03
ORD IDord-240e1322ffa64302acd2fb0355bdeede
Source noteuspto-grants-2013_03