HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699566Generated: November 1, 2026
HCID 70110358, compound → HCID 18707303, compound
https://huagongshe.com/reaction/1699566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 70110358 | HCID 70110358 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18707303 | HCID 18707303 | 160.4% |
Reaction Steps
To a solution of 1 g of 2-(3,4-diethoxyphenyl)-4-(3-methoxycarbonyl-4-hydroxy-4-allylphenyl)thiazole in 20 ml of methanol and 20 ml of tetrahydrofuran were added 0.5 ml of osmium tetroxide (a 4% aqueous solution) and 1.22 g of4-methylmorpholine N-oxide. The mixture was stirred at room temperature for 4 hours. The solvent was removed by distillation. The residue was mixed with 50 ml of dichloromethane and 25 ml of water for phase separation. The organic layer was washed with 25 ml of a saturated aqueous sodium chloride solution and dried. The solvent was removed by distillation. The residue was purified by silica gel column chromatography (eluent: dichloromethane/methanol=199/1) to obtain 860 mg of 2-(3,4-diethoxyphenyl)-4-(3-methoxycarbonyl-4-hydroxy-5-(2,3-dihydroxypropyl)phenyl]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE037556E1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-8a4b23440ca44ccd9b22f57f0d24c110 |
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| Source note | uspto-grants-2002_02 |
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