HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838789Generated: November 2, 2026
Water → 2,3-Dimethylpent-3-yl allyl carbonate
https://huagongshe.com/reaction/838789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,3-Dimethylpentan-3-ol | HCID 11685 | — |
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Dimethylpent-3-yl allyl carbonate | HCID 20384470 | 53.9% |
Reaction Steps
To a solution of 11.62 grams (0.1 mole) of 2,3-dimethylpentan-3-ol in 75 milliliters of anhydrous tetrahydrofuran at 0° C was added one equivalent of methyllithium in diethyl ether, followed by 12.1 grams (0.10 mole) of allyl chloroformate in 25 milliliters of anhydrous tetrahydrofuran. During both additions the temperature was maintained at 0° C. After the last addition was complete the reaction mixture was stirred for about 18 hours and allowed to warm to ambient temperature. The reaction mixture was poured into water, and then extracted with ether. The ether solution was washed four times with water and dried over magnesium sulfate. Removal of solvent under reduced pressure yielded 18.27 grams (93.1% crude yield) of a yellow oil. Vacuum distillation gave 10.79 grams of 2,3-dimethylpent-3-yl allyl carbonate, b.p. 59°-60° C/0.15 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04092988 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-ab4cdb8115e948d8b76618b248b2a44c |
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| Source note | uspto-grants-1978_06 |
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