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HRID 341861作成日:2026年10月27日

Chloromethyl Methyl Ether → 4-(Methoxymethyloxy)-phenyldisulfide

https://huagongshe.com/reaction/341861

反応式

関与物質

役割名称HCID仕込み量
反応物Chloromethyl Methyl EtherHCID 7864—
反応物Sodium hydrideHCID 24758—
反応物4-[(4-Hydroxyphenyl)disulfanyl]phenolHCID 280665—
反応物Brine ethyl acetateHCID 131718255—
溶媒DimethylformamideHCID 6228—
生成物4-(Methoxymethyloxy)-phenyldisulfideHCID 88220868—

反応手順

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) d 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05856339
出典データセットuspto-grants-1999_01
ORD IDord-a421308b36874487ae9ba946177ff79a
出典メモuspto-grants-1999_01