HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzhydrylamine → 2-Bromo-N-(diphenylmethyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Product | 2-Bromo-N-(diphenylmethyl)acetamide | HCID 14185948 | 19.4% |
Reaction Steps
A solution of 2.91 g (14.39 mmol) of bromoacetyl bromide in 40 ml was cooled to 0° C. and 2.1 ml (14.39 mmol) of triethylamine and 2.64 g (14.39 mmol) of benzhydrylamine were successively added. The reaction solution was then evaporated to dryness under reduced pressure, and the resulting residue was purified on silica gel with EA as mobile phase. The product crystallized from the product fractions was filtered off with suction, washed with a little cold diethyl ether and dried under reduced pressure, resulting in 0.85 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710232B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-9be0440c64284ba4861e43624e54de49 |
| Source note | uspto-grants-2014_04 |