HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 4-(6-Bromohexyl)-3-(3-ethoxy-3-oxopropyl)benzenepentanoic Acid Ethyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(3-Ethoxy-3-oxopropyl)-4-(6-hydroxyhexyl)benzenepentanoic acid ethyl ester | HCID 53721985 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(6-Bromohexyl)-3-(3-ethoxy-3-oxopropyl)benzenepentanoic Acid Ethyl Ester | HCID 54295390 | 75.9% |
Reaction Steps
A mixture of 0.673 g (1.65 mmol) of 3-(3-ethoxy-3-oxopropyl)-4-(6-hydroxyhexyl)benzenepentanoic acid ethyl ester from the preceding example, 1.1 g (3.3 mmol) of carbon tetrabromide, and 0.9 g (3.3 mmol) of triphenylphosphine in 25 mL of ether was stirred at room temperature for 23 hr. The mixture was diluted with 250 mL of ether, and the solution worked-up in the usual manner. The crude product was purified by flash chromatography on 80 g of silica gel, eluting with hexane-ethyl acetate (10:1). There was obtained 0.588 g (75.7%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434186 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-32be5f95d38f4c4896a30df41147d917 |
| Source note | uspto-grants-1995_07 |