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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7,8-Difluorochroman-6-ol | HCID 59215241 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7,8-Difluoro-6-methoxymethoxychroman | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678929B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-85681d7a6e1d4957b3d513ddb39ede20 |
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| Source note | uspto-grants-2010_03 |
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