HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733341Generated: October 29, 2026
Chloromethyl Methyl Ether → 3-(4-Benzyloxy-2-methoxymethoxyphenyl)propionamide
https://huagongshe.com/reaction/733341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(4-Benzyloxy-2-hydroxyphenyl)propionamide | HCID 17856263 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Benzyloxy-2-methoxymethoxyphenyl)propionamide | HCID 17856235 | — |
Reaction Steps
To a stirred suspension of 5.64 g of 60% sodium hydride in oil in 628 mL of N,N-dimethylformamide was added 34.8 g of 3-(4-benzyloxy-2-hydroxyphenyl)propionamide under ice-cooling, and the mixture was stirred at 50° C. for 40 minutes. To the reaction mixture was added 12.39 g of chloromethyl methyl ether under ice-cooling, and the mixture was stirred at room temperature for 15 hours. After the reaction mixture was concentrated under reduced pressure to remove the solvent, the residue was poured into a mixture of 500 mL of ethyl acetate, 100 mL of toluene, and 200 mL of water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to give a colorless solid. The solid was triturated in ethyl acetate-diisopropyl ether to collect by filtration of 35.3 g of 3-(4-benzyloxy-2-methoxymethoxy-phenyl)propionamide as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589126B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-19d2f38f56fa47a08da8ec298be988f2 |
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| Source note | uspto-grants-2009_09 |
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