HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivaloyl chloride → Ethyl 6-chloro-2-fluoro-3-(pivalamidomethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Ethyl 3-(aminomethyl)-6-chloro-2-fluorobenzoate | HCID 58483233 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 6-chloro-2-fluoro-3-(pivalamidomethyl)benzoate | HCID 58483442 | 63.3% |
Reaction Steps
To a solution of ethyl 3-(aminomethyl)-6-chloro-2-fluorobenzoate (0.540 g, 2.5 mmol) in THF (5 mL) was added pivaloyl chloride (0.335 g, 2.79 mmol) and TEA (0.1 mL) and the reaction mixture was stirred for 2-3 h at RT. Excess of solvent was removed under vacuum and the residue was diluted with water, extracted with EtOAC and concentrated to afford 0.500 g of the product. 1H NMR (300 MHz, DMSO d6): δ 1.11 (s, 9H), 1.31 (t, J=7.5 Hz, 3H), 4.26 (d, J=5.1 Hz, 2H), 4.39 (q, J=6.6 Hz, 2H), 7.33-7.43 (m, 2H), 8.13 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09439890B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-679e0785981e4a348fc8c897ec2e048e |
| Source note | uspto-grants-2016_09 |