HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → tert-Butyl 3-bromobenzyl(methyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl 3-bromobenzylcarbamate | HCID 11033439 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 3-bromobenzyl(methyl)carbamate | HCID 20738487 | — |
Reaction Steps
128 g (447 mmol) of tert-butyl (3-bromobenzyl)carbamate and 800 ml of DMF are introduced into a round-bottomed flask and under a nitrogen stream. 19 g (475 mmol) of sodium hydride (60% in oil) are added in small quantities and the mixture is stirred until the gas emission ceases. 29.3 ml (470 mmol) of methyl iodide are then added and the mixture is stirred overnight. The reaction medium is poured into ice-cold water, extracted with ethyl acetate, the organic phase decanted off, dried over magnesium sulphate and evaporated off. 152.5 g (92%) of the expected product are recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07294639B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-3397b448857f49ebaf9dbdecc2995024 |
| Source note | uspto-grants-2007_11 |