HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486959Generated: October 30, 2026
Thioglycolic Acid → HCID 14514935, compound
https://huagongshe.com/reaction/486959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 53784355 | HCID 53784355 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 14514935 | HCID 14514935 | 92.9% |
Reaction Steps
1.2 g of α-(6-isopropyl-1,3-benzodioxol-5-yl)benzyl alcohol was dissolved in 10 ml of benzene, followed by the addition of 490 mg of mercaptoacetic acid and a catalytic amount of p-toluenesulfonic acid monohydrate. The obtained mixture was heated under reflux for one hour and cooled, followed by the addition of benzene. The mixture was washed with water, followed by the addition of a 1N aqueous solution of sodium hydroxide. The alkaline layer was separated, acidified with concentrated hydrochloric acid and extracted with chloroform. The extract was washed with water, dried over anhydrous magnesium sulfate and filtered. The filtrate was distilled to remove the solvent. The residue was purified by silica gel column chromatography (hexane/chloroform=3:7) to obtain 1.42 g of the title compound as a colorless prismatic crystal.
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-5ef9547f5bab4af08762ba5771b9e67e |
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| Source note | uspto-grants-1994_03 |
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