HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → HCID 12517307, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 12517303 | HCID 12517303 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12517307 | HCID 12517307 | 87.3% |
Reaction Steps
To a stirred mixture of 56 g (0.163 mole) of 2-amino-5-chloro-4'-(2,2,2-trifluoroacetamido)-benzophenone in 900 ml of ether was added 43 g (0.213 mole) of bromoacetyl bromide and a saturated aqueous solution of sodium bicarbonate in portions, keeping the solution slightly basis during the addition. The reaction was stirred for 90 min and filtered to give 66 g of product. The ether layer was dried and evaporated and the residual oil was crystallized from methanol to give an additional 10 g of the product for a total yield of 76 g (96%). Recrystallization from a mixture of dichloromethane, methanol and petroleum ether gave an analytical sample of off white rods, mp 198°-201° ir (KBr) 1750, 1663, 1640 cm-1 (3C=O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04083948 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-cf1fcc11b0234f4eabd2aa8cfe3019ef |
| Source note | uspto-grants-1978_04 |