HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-(2-bromoethyl)-4-methoxy-2-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Reactant | 4-Methoxy-2-nitrobenzoyl chloride | HCID 21474053 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-bromoethyl)-4-methoxy-2-nitrobenzamide | HCID 13476532 | 68% |
Reaction Steps
To a stirred and cooled (ice-bath) solution of 27.5 parts of 2-bromoethanamine hydrobromide in 200 parts of water is added a solution of 28.9 parts of 4-methoxy-2-nitrobenzoyl chloride in 63 parts of benzene at 5°-10° C. While stirring vigorously, there is added dropwise a solution of 10.8 parts of sodium hydroxide in 250 parts of water at 5°-10° C. Upon completion, stirring is continued for 2 hours at this temperature. The supernatant phase is decanted and the oily residue is stirred in 2-propanol. The product is filtered off and dried, yielding 27.5 parts (68%) of N-(2-bromoethyl)-4-methoxy-2-nitrobenzamide; mp. 133.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04522945 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-82f0ddc216704c49ad26b788b03abb2f |
| Source note | uspto-grants-1985_06 |