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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307155Generated: October 31, 2026

(+/-)-N-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}methanesulfonamide → (+/-)-N-[3-(2,4-Dihydroxyphenyl)cyclohexyl]methanesulfonamide

https://huagongshe.com/reaction/2307155

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-N-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}methanesulfonamideHCID 22337797—
SolventMethanolHCID 887—
Product(+/-)-N-[3-(2,4-Dihydroxyphenyl)cyclohexyl]methanesulfonamideHCID 979584338.5%

Reaction Steps

(±)-N-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}methanesulfonamide (34 mg) was heated under reflux in methanol (2 ml) containing acidic ion exchange resin (0.3 g) for 5 hr. The reaction mixture was filtered and the resin was washed with methanol. The combined filtrate and washings were evaporated in vacuo and the crude residue was purified by preparative HPLC to furnish a mixture of diastereoisomers of the title compound as a pale pink solid (10 mg, 38%). δH (d4-MeOH) 1.20-2.00 (7H, overlapping m), 2.07 (1H, m), 2.90 (0.5H, m), 2.93 (1.5H, s), 2.97 (1.5H, s), 3.13 (0.5H, m), 3.30 (0.5H, m), 3.80(0.5H, m), 6.21-6.26 (1H, dd), 6.87 (0.5H, d), 6.89 (0.5H, d); m/z (ES−) 284 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828460B2
Source datasetuspto-grants-2004_12
ORD IDord-4233f84a7f8f4b4f91e0c2339cade3de
Source noteuspto-grants-2004_12