HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520433Generated: October 31, 2026
Dichloromethane → ethyl 2-hydroxy-2-methylpent-4-enoate
https://huagongshe.com/reaction/520433
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl pyruvate | HCID 12041 | — |
| Reactant | Allyltrimethylsilane | HCID 69808 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Product | ethyl 2-hydroxy-2-methylpent-4-enoate | HCID 10909832 | 58.7% |
Reaction Steps
Ethyl 2-oxopropanoate (1 g, 8.61 mmol) was taken in to DCM (5M) and cooled to −78 C. To this titanium tetrachloride (8.61 mL, 8.61 mmol) in dichloromethane (5 mL) was added and stirred the reaction mixture for 30 min at this temperature. To this reaction mixture allyltrimethylsilane (1.279 g, 11.20 mmol) was added drop wise at −78° C. and stirring was continued for 2 h. Then it was brought to 0° C. and quenched with saturated aq. sodium bicarbonate solution and stirred for 15 min, and filtered through celite bed and filtrate was evaporated under reduced pressure to afford colorless oil. The residue was purified by flash chromatography (silica, 230-400, 10% EtoAc/Pet ether) to obtain ethyl 2-hydroxy-2-methylpent-4-enoate B-37a (0.8 g, 5.06 mmol, 58.7% yield) as yellow liquid. 1H NMR (CDCl3, δ=7.26 ppm, 400 MHz): δ 5.84-5.72 (m, 1H), 5.15-5.09 (m, 2H), 4.29-4.19 (m, 2H), 2.56-2.37 (m, 2H), 1.43 (s, 3H), 1.31 (t, J=9.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326973B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-93eacaec2d724974a9c3e36db47660bb |
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| Source note | uspto-grants-2016_05 |
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