HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43305Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 56949563, compound
https://huagongshe.com/reaction/43305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl tiglate | HCID 5281163 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 56949563 | HCID 56949563 | 93.4% |
Reaction Steps
A mixture of 51.27 g (0.40 mol) of ethyl tiglate, 76.12 g (1.00 mol) of thioacetic acid, and 7.60 g (0.04 mol) of para-toluenesulfonic acid was stirred under nitrogen atmosphere at 75° C. for 24 hours. After cooling, diethyl ether and a saturated aqueous sodium bicarbonate solution were added to the reaction mixture. The organic layer was separated and washed twice with brine. The solvent in the organic layer was evaporated off, and vacuum distillation (68 to 71° C./2 torr) was performed to give 76.36 g of the objective compound (GC purity: 98.3%, yield: 91.8%, diastereomer ratio: 80.9/19.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536364B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-016ffa8300174900b07aef8aef472a85 |
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| Source note | uspto-grants-2013_09 |
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