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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585693Generated: October 29, 2026

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

https://huagongshe.com/reaction/585693

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 numberUS06933319B2
Source datasetuspto-grants-2005_08
ORD IDord-719b8138519c42a5b68bae5e953811a1
Source noteuspto-grants-2005_08