HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Ethyl 1-(2-bromoacetyl)cyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 1-acetylcyclopropane-1-carboxylate | HCID 234183 | — |
| Product | Ethyl 1-(2-bromoacetyl)cyclopropanecarboxylate | HCID 11436266 | 71% |
Reaction Steps
To a 100 mL of round-bottomed flask was added ethyl 1-acetylcyclo-propanecarboxylate (15.6 g, 100 mmol) and NBS solid (21.36 g, 120 mmol), followed by p-toluene sulfonic acid (1.9 g, 10 mmol). After stirring at rt for 8 hrs, the reaction mixture was extracted with diethyl ether (200 mL) and washed with 80 mL of water. The organic phase was then dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (1:30(v/v)EtOAc/n-hexane) to give the title compound as colorless oil (16.68 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293897B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-08c8661327e34bfb8920324541adf2be |
| Source note | uspto-grants-2012_10 |