HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 2-(4-Bromophenoxy)acetohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | p-Bromophenoxyacetic acid | HCID 74657 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Bromophenoxy)acetohydrazide | HCID 692241 | — |
Reaction Steps
To a solution of (4-bromophenoxy)acetic acid (1.0 g, 4.3 mmol) in THF (15 mL) was added N,N-Carbonyldiimidazole (0.84 g, 5.2 mmol). After refluxing for 2 hours, hydrazine (0.6 g, 20 mmol) was added to the reaction mixture slowly with a syringe at 0° C. The reaction mixture was allowed to warm to room temperature slowly and then concentrated to yield the desired product as a white solid. LCMS calculated for C8H10BrN2O2 (M+H): 245.0; found: 244.9, 246.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462624B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-6eeb18d12e984242b1a97137596d1b25 |
| Source note | uspto-grants-2008_12 |