HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745894Generated: October 31, 2026
Chloromethyl Methyl Ether → HCID 22227320, compound
https://huagongshe.com/reaction/1745894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | 5-Hydroxy-2-pentanone | HCID 14066 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22227320 | HCID 22227320 | 75.2% |
Reaction Steps
Compound 27 intermediates: To diisopropylethyl amine (18.48 g, 143 mmol) in 200 mL of dichloromethane was added 3-acetyl-1-propanol (13.28 g, 130 mmol) at 0° C. After the solution was stirred for 0.5 hour, chloromethylmethyl ether (13.08 g, 162.5 mmol) was added while the temperature was maintained at 0° C. The resulting solution was stirred for another 1 hour, brought to room temperature and stirred overnight. Organic solvent was removed via rotary evaporation. The residue was treated with 100 mL of brine and extracted with 3×150 mL of diethyl ether. The organic layers were combined, dried over Na2SO4 and concentrated via rotary evaporation. The crude product was purified via a flash chromatography with dichloromethane as eluent to afford 5-methoxymethoxy-2-pentanone (14.3 g, yield: 75) as a pale oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019453B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-3e3fe36490f8493fbebc92f863b914bc |
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| Source note | uspto-grants-2006_03 |
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