HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → N'-(2-chloroacetyl)-3-cyanobenzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Cyanobenzohydrazide | HCID 21942658 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N'-(2-chloroacetyl)-3-cyanobenzohydrazide | HCID 54595588 | 69% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3-cyanobenzohydrazide (1.6 g, 10.0 mmol) was added to THF (40 ml) and DMF (10 ml). TEA (1.4 ml, 10.0 mmol) was added at 0° C. followed by chloroacetyl chloride (1.0 ml, 12.6 mmol) and the reaction mixture was stirred at 0° C. for 1 h and at rt for 2 h. The THF was evaporated, water was added to the remaining mixture, followed by filtratation over celite and purification with prep. HPLC to give the title compound (1.6 g, 69%). 1H NMR (DMSO-d6): 10.62 (br s, 2 H), 8.28 (m, 1 H), 8.18 (m, 1 H), 8.08 (m, 1 H), 7.75 (t, 1 H), 4.22 (s, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585881B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-d846238eb2fb48888bece67cafb46889 |
| Source note | uspto-grants-2009_09 |