HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-[(5-Bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-[2-[(5-Bromopentyl)oxy]-5-chlorophenyl]-2-propenoic acid methyl ester | HCID 53828054 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[(5-Bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl ester | HCID 54391460 | 100.8% |
Reaction Steps
A mixture of 2.02 g (5.59 mmol) of 3-[2-[(5-bromopentyl)oxy]-5-chlorophenyl]-2-propenoic acid methyl ester (mixture of E/Z isomers), 90 mL of tetrahydrofuran, 190 mL of toluene, and 1.26 g of 5% rhodium on alumina was stirred at room temperature, in an atmosphere of hydrogen, until reduction was complete. The catalyst was removed by suction filtration and the filtrate was concentrated in vacuo giving 2.05 g (ca. 100%) of 2-[(5-bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl ester as a pale-yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273999 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-7239bf6c1db74d52b599f4d574a48ecf |
| Source note | uspto-grants-1993_12 |