HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl N-methoxymethyl-N-(3-phenylbenzyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethyl methyl ether | HCID 83093 | — |
| Reactant | methyl N-(3-phenylbenzyl)carbamate | HCID 12090300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl N-methoxymethyl-N-(3-phenylbenzyl)carbamate | HCID 12090306 | 76.1% |
Reaction Steps
1.00 g of methyl N-(3-phenylbenzyl)carbamate in tetrahydrofuran (20 ml) was stirred together with 0.22 g of 60% sodium hydride at room temperature for 30 minutes. 0.78 g of methoxymethyl bromide was added dropwise at room temperature, and the resulting solution was stirred overnight. After the reaction, the reaction solution was poured into water and extracted with ethyl acetate, and the organic layer was separated, dried over anhydrous magnesium sulfate and evaporated under reduced pressure for removal of the solvent. The residue was purified by silica gel column chromatography to give 0.90 g of methyl N-methoxymethyl-N-(3-phenylbenzyl)carbamate as a pale yellow transparent viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06620961B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-a241719dc28248dcb5e7c404b29c52ec |
| Source note | uspto-grants-2003_09 |