HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioglycolic Acid → [{1-(6-Methyl-1,3-benzodioxol-5-yl)propyl}thio]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | 1-(6-Methylbenzo[d][1,3]dioxol-5-yl)propan-1-ol | HCID 14514897 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | [{1-(6-Methyl-1,3-benzodioxol-5-yl)propyl}thio]acetic acid | HCID 14514911 | 90.2% |
Reaction Steps
2.27 g of 1-(6-methyl-1,3-benzodioxol-5-yl)-1-propanol, 0.1 g of p-toluenesulfonic acid and 1.52 g of mercaptoacetic acid were dissolved in 80 ml of benzene to obtain a solution. This solution was heated under reflux for 12 hours, while removing generated water. The reaction mixture was poured into water. The aqueous layer was basified and washed with ether. The aqueous layer was acidified and extracted with chloroform. The organic layer was washed with water, dried over magnesium sulfate and concentrated in a vacuum to obtain a pale yellow solid. This solid was purified by silica gel column chromatography (ethyl acetate/hexane=2:8) to obtain 2.83 g of the title compound as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292901 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-75705dd5e4e64dfabc0404011fd65e95 |
| Source note | uspto-grants-1994_03 |