HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064832Generated: October 31, 2026
Potassium ethylxanthate → HCID 178497335, compound
https://huagongshe.com/reaction/1064832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Reactant | Dimethyl 3-hydroxy-4-nitrophthalate | HCID 22272660 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178497335 | HCID 178497335 | 60% |
Reaction Steps
A 10% palladium carbon catalyst (2.5 g) was added to a solution of the nitro compound mixture (4.3 g, 16.8 mmol) in ethyl acetate (60 ml) and stirred under hydrogen atmosphere at room temperature for 3 hours. The reaction solution was filtered off through celite and the filtrate was concentrated. The residue was dissolved in methanol (50 ml), potassium O-ethyl dithiocarbonate (1.76 g, 11.0 mmol) was added thereto and the mixture was heated to reflux for 16 hours. After cooling, the solvent was evaporated in vacuo. The residue was diluted and acidified with 2N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water and a saturated sodium chloride solution successively and dried over anhydrous magnesium sulfate and the solvent was evaporated therefrom. The residue was crystallized from ether to provide 1.61 g (yield 60%) of 6,7-bis(methoxycarbonyl)-2-mercaptobenzooxazole as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06969711B2 |
|---|
| Source dataset | uspto-grants-2005_11 |
|---|
| ORD ID | ord-835ff2db093f43c4aa25f7e894eb421f |
|---|
| Source note | uspto-grants-2005_11 |
|---|