HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466271Generated: October 29, 2026
Acetic acid, 2-oxo-, methyl ester → HCID 19873328, compound
https://huagongshe.com/reaction/466271
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, 2-oxo-, methyl ester | HCID 70205 | — |
| Reactant | HCID 53675796 | HCID 53675796 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 19873328 | HCID 19873328 | 36% |
Reaction Steps
In the same manner as in Example 1, a solution of an (R)-binaphthol-dichlorotitanium complex was obtained. This solution was cooled to -70° C. in a dry ice-acetone bath. To this solution were successively added 88 mg (1 mmole) of methyl glyoxylate and 282 mg (2 mmole) of 1-dimethylaminocarbonyloxy-1,3-butadiene. Reaction was then allowed to proceed at -30° C. for 10 hours, and 10 ml of a sodium hydrogencarbonate aqueous solution was added to the reaction mixture to terminate the reaction. This reaction mixture was filtered through Celite and then subjected to extraction once with 20 ml of diethyl ether and twice with 20 ml of ethyl acetate. The extract was dried over anhydrous magnesium sulfate. Thereafter, the solvent was removed by evaporation, and the residue was purified by silica gel column chromatography (200 mesh; developing solvent: hexane/ethyl acetate=10/1), thereby obtaining 82 mg of desired optically active 6-methoxycarbonyl-2-dimethylaminocarbonyloxy-5,6-dihydropyran (yield: 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155240 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-0ab0715e22c24e13bd38bce8c3d1a7ff |
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| Source note | uspto-grants-1992_10 |
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