HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21069807, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21069806 | HCID 21069806 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ammonia methanol | HCID 21705897 | — |
| Product | HCID 21069807 | HCID 21069807 | — |
Reaction Steps
A solution of 2,5-dibromo-4-fluorobenzyl bromide (0.350 g, 1 mmol) in 7M NH3/MeOH was heated in a sealed tube at 100° C. for 2 h. The reaction mixture was cooled and concentrated to give a white solid which was dissolved in CH2Cl2 and treated with Et3N (1 mL) then concentrated. The resulting residue was triturated with ethyl acetate (25 mL), filtered and concentrated to give the title compound (0.291 g) as a pale yellow oil. HRMS (M+H) calcd for C7H7Br2FN: 283.94; found: 283.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07176196B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-1ada92e2ebdd49fe8767123cc9c9b450 |
| Source note | uspto-grants-2007_02 |