HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 5-(2-Bromoacetyl)pyrazole-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Reactant | HCID 178468948 | HCID 178468948 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Bromoacetyl)pyrazole-3-carboxylic acid ethyl ester | HCID 178469076 | 145.7% |
Reaction Steps
A 100ml flask was charged with 27.8 g of 5-acetylpyrazole-3-carboxylic acid ethyl ester and 40 ml of tetrahydrofuran. To this mixture, 56.4 g of phenyltrimethylammonium tribromide were added. The resulting red mixture was stirred at room temperature for 1 hour and poured into 600 ml of water. The resulting mixture was filtered and the solids were washed with more water. The solids were collected, air-dried and recrystallized from 1:1 mixture of disopropyl ether and hexanes (300ml) to afford 33.1 g of 5-(2-bromoacetyl)pyrazole-3-carboxylic acid ethyl ester as white solids, mp 174°-176° C. NMR: 1.42 (t, 3H), 4.44 (q, 2H), 4.57 (s, 2H), 7.4 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05470862 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-40a3b2b9e5c448a0ad925245d4f739eb |
| Source note | uspto-grants-1995_11 |