HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979289Generated: October 31, 2026
Chloromethyl Methyl Ether → HCID 21201664, compound
https://huagongshe.com/reaction/1979289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 16640186 | HCID 16640186 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21201664 | HCID 21201664 | 99% |
Reaction Steps
In an argon stream, 2-oxo-5-phenyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (40.4 g) was added to 60% sodium hydride (8.84 g) suspended in absolute tetrahydrofuran (500 ml) at 0° C. The mixture was stirred for one hour at 0° C., and chloromethyl methyl ether (20.5 g) was added thereto, followed by stirring for two hours and 30 minutes at room temperature. The reaction mixture was concentrated under reduced pressure, and ice-water was added thereto, followed by extraction with chloroform. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, to thereby obtain 47.4 g of the title compound as a yellow oil (yield: 98.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06239131B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-929cba91cd534189b7635e2ccf779b73 |
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| Source note | uspto-grants-2001_05 |
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