HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triclosan → 5-Chloro-2-(2,4-dichlorophenoxy)phenyl 4-carboxy-3-methylbutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triclosan | HCID 5564 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methylglutaric anhydride | HCID 77828 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Chloro-2-(2,4-dichlorophenoxy)phenyl 4-carboxy-3-methylbutyrate | HCID 23322896 | 23% |
Reaction Steps
A mixture of triclosan (22.3 g.), 3-methylglutaric anhydride (15.0 g.) and triethylamine (15 ml.) in ether (250 ml.) was stirred for 20 hours, and then washed first with 2M hydrochloric acid (50 ml.) and then with water (3×150 ml.). The ether phase was dried (MgSO4) and evaporated. A portion (20 g.) of the residual oil was purified by chromatography on silica gel using methylene chloride as eluant to give (D) as a colourless oil (7.4 g.) ; NMR (CDCl3): 0.8-1.3 (3H,d, CH3), 2.1-2.8 (5H,m,CH2CO+CH3CH), 6.7-7.6 (6H, m, aromatic H), 11.25 (1H,s, CO2H)ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587262 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-9c22268e69f445f58f3de5e07ed5e4a6 |
| Source note | uspto-grants-1986_05 |