HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486848Generated: October 25, 2026
Methanol → Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester
https://huagongshe.com/reaction/486848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | (+)-2,2-Dimethyl-(3-chloro-2-hydroxypropyl)-1,3-dioxin-4-one | HCID 19096633 | — |
| Product | Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester | HCID 4377704 | 66% |
Reaction Steps
Ozone was introduced into a mixture of 225.5 mg (1 mmol) of (+)-2,2-dimethyl-(3-chloro-2-hydroxypropyl)-1,3-dioxin-4-one (96% ee) obtained in Example 4 and 20 ml of methanol at -78° C. for 5 hours, and 2 ml of dimethyl sulfide were added thereto, followed by stirring at the same temperature for 2 hours. The temperature was gradually returned to room temperature, and the solution was then stirred for 5 hours. Afterward, the solvent was distilled off, and the resultant residue was then dissolved in ethanol. 3 drops of concentrated sulfuric acid were added thereto, and the solution was then heated at 80° C. for 30 minutes. Next, ethanol was distilled off, and the residue was diluted with water. The solution was extracted with dichloromethane and then dried over anhydrous sodium sulfate, and the solvent was distilled off and the residue was then subjected to column chromatography (an eluent of hexane:ethyl acetate=5:1), thereby obtaining 109.4 mg (yield 66%) of (+)-ethyl 4-chloro-3-hydroxybutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292891 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-d4141169b3a64ab4b95d97dc751e2fd7 |
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| Source note | uspto-grants-1994_03 |
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