HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382525Generated: October 31, 2026
Chloromethyl Methyl Ether → HCID 68649319, compound
https://huagongshe.com/reaction/2382525
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | HCID 14456327 | HCID 14456327 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 68649319 | HCID 68649319 | — |
Reaction Steps
A solution of annonacinone (595 mg, 1.0 mmol) in diisopropylethylamine (7 mL) is stirred at room temperature while chloromethyl methyl ether (360 mg, 4.5 mmol) is added. The mixture is stirred at room temperature for eight hours, concentrated in vacuo, and the residue is partitioned between water (50 mL) and ethyl acetate (50 mL). The aqueous phase is separated and extracted with ethyl acetate (2×50 mL) and the combined organic fractions are washed (1× water), dried (saturated aqueous NaCl, sodium sulfate), filtered, and concentrated. Chromatography (hexane-2:1 hexane:ethyl acetate gradient over silica gel 230-400 mesh) affords 3-{2,13-bis(methoxymethyloxy)-13-[tetrahydro-5-(1-methoxymethyloxytridecyl)furan-2-yl]tridecan-8-on-1-yl}-5-methyl-2-(5H)-furanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263042B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-8d1d430c200844bfab2ebdc632c93d56 |
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| Source note | uspto-grants-2012_09 |
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