HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioglycolic Acid → [{1-(6-Methyl-1,3-benzodioxol-5-yl)ethyl}thio]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | 1-(6-Methyl-1,3-benzodioxol-5-yl)ethanol | HCID 14514896 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | [{1-(6-Methyl-1,3-benzodioxol-5-yl)ethyl}thio]acetic acid | HCID 14514909 | 93% |
Reaction Steps
3.7 g of mercaptoacetic acid and a catalytic amount of D-10-camphorsulfonic acid were added to 3.2 g of 1-(6-methyl-1,3-benzodioxol-5-yl)ethanol and the mixture was heated under reflux in 100 ml of benzene for 1 h. The reaction mixture was washed with water and then extracted with a 1 1Nsodium hydroxide solution. The aqueous layer was washed with ethyl acetate, acidified with 1Nhydrochloric acid and extracted with chloroform. The organic layer was dried over magnesium sulfate and the solvent was distilled off to obtain a crystalline residue. After recrystallization from diisopropyl ether, 4.2 g of the intended compound was obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05110956 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-129ac101307246a3975f80d3d5ac4c8d |
| Source note | uspto-grants-1992_05 |