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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115920Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 86599068, compound

https://huagongshe.com/reaction/2115920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68966163HCID 68966163—
ReactantHCID 86599067HCID 86599067—
ProductHCID 86599068HCID 8659906869%

Reaction Steps

Treatment of 2-allyl-4-chloro-6-isopropyl-3-methylphenol (8.88 g, 0.04 mmol) with 3-chloroperoxybenzoic acid (13.63 g, 0.079 mol, 77%)) followed by potassium carbonate (10.92 g, 0.079 mol) generally according to the procedure described for Intermediate 9 provided (±)-(5-chloro-7-isopropyl-4-methyl-2,3-dihydro-1-benzofuran-2-yl)methanol. Treatment of (±)-(5-chloro-7-isopropyl-4-methyl-2,3-dihydro-1-benzofuran-2-yl)methanol (5.95 g, 0.025 mol) with p-toluenesulfonyl chloride (5.66 g, 0.03 mol) generally according to the procedure described for Intermediate 10 afforded 6.71 g (69%) (±)-(5-chloro-7-isopropyl-4-methyl-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate as a white solid. mp 103-105° C.; Anal. calcd. for C20H23ClO4S C, 60.83; H, 5.87. Found C, 60.67; H, 5.88.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-378f36bf510644989dd51256b7b35401
Source noteuspto-grants-2008_10