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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375827Generated: October 25, 2026

Chloromethyl Methyl Ether → HCID 88220868, compound

https://huagongshe.com/reaction/375827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant4-[(4-Hydroxyphenyl)disulfanyl]phenolHCID 280665—
ReactantBrine ethyl acetateHCID 131718255—
SolventDimethylformamideHCID 6228—
ProductHCID 88220868HCID 88220868—

Reaction Steps

To a solution of 4-hydroxyphenyldisulfide (650 mg, 2.60 mmol) in 10 mL of anhydrous N,N-dimethylformamide at 10° C. was added sodium hydride (230 mg, 5.75 mmol, 60% dispersion in mineral oil). After stirring for 15 minutes, chloromethylmethyl ether (0.44 mL, 5.75 mmol) was added via syringe. The reaction was warmed to ambient temperature and stirred for 0.5 hours. The mixture was distributed between brine/ethyl acetate (20 mL each). The layers were separated and the aqueous phase extracted with ethyl acetate (2×20 mL). The organic was dried (sodium sulfate) and concentrated to a yellow oil (993 mg, 100%). An analytical sample of 4-(methoxymethyloxy)-phenyldisulfide was prepared by chromatography (silicon dioxide, 4% ethyl acetate/hexanes). 1H NMR (DMSO-d6) δ 7.40 (d, J=6.9 Hz, 4H), 7.00 (d, J=6.9 Hz, 4H), 5.15 (s, 4H), 3.32 (s, 6H). FD mass spec: 338. Anal. Calcd. for C16H18O4S2 : C, 56.78; H, 5.36. Found: C, 57.08; H, 5.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488058
Source datasetuspto-grants-1996_01
ORD IDord-e88901911db34d179455a3eccd9fbb41
Source noteuspto-grants-1996_01