HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486895Generated: October 27, 2026
Thioglycolic Acid → [{2-(1,3-Benzodioxol-5-yl)-2-propyl}thio]acetic acid
https://huagongshe.com/reaction/486895
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | 2-(Benzo[d][1,3]dioxol-5-yl)propan-2-ol | HCID 11819632 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | [{2-(1,3-Benzodioxol-5-yl)-2-propyl}thio]acetic acid | HCID 14514907 | 45.8% |
Reaction Steps
600 ml of benzene, 59.5 g of mercaptoacetic acid and a catalytic amount of D-10-camphorsulfonic acid were added to 97 g of 2-(1,3-benzodioxol-5-yl)-2-propanol and the mixture was heated under reflux for 4 h. The solvent was distilled off and the pH of the residue was adjusted to 10 with 1N aqueous sodium hydroxide solution. After washing with ethyl acetate, 4N hydrochloric acid was added thereto under cooling with ice to acidify the aqueous layer. After extraction with chloroform, the extract was washed with water and dried over anhydrous magnesium sulfate. It was filtered and the filtrate was concentrated. The crystals thus formed were recrystallized from diisopropyl ether to obtain 62.70 g of the intended compound in the form of colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292901 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-b4e04dae3d364c879e13080143fdc58d |
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| Source note | uspto-grants-1994_03 |
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