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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244830Generated: November 1, 2026

Chloromethyl Methyl Ether → 7,8-Difluoro-6-methoxymethoxychroman

https://huagongshe.com/reaction/2244830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantTriethylamineHCID 8471—
ReactantDiisopropylethylamineHCID 81531—
Reactant7,8-Difluorochroman-6-olHCID 59215241—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product7,8-Difluoro-6-methoxymethoxychromanHCID 59215258—

Reaction Steps

15.0 g (80.6 mmol) of 7,8-difluorochroman-6-ol are dissolved in 135 ml of dichloromethane, and 16.5 ml (94.2 mmol) of N-ethyldiisopropylamine are added with ice-cooling. After 5 min, 7.34 ml (97.0 mmol) of chloromethyl methyl ether are metered in the temperature range from 15 to 30° C. After 18 h at 20° C., 50 ml of triethylamine are added, and the batch is stirred again for 18 h. Water is added to the reaction mixture, and the organic phase is separated off. The aqueous phase is extracted with dichloromethane, and the combined organic phases are washed successively with water and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane:MTBE=2:1), giving 7,8-difluoro-6-methoxymethoxychroman as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678929B2
Source datasetuspto-grants-2010_03
ORD IDord-85681d7a6e1d4957b3d513ddb39ede20
Source noteuspto-grants-2010_03