HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441841Generated: October 25, 2026
3-Chloro-2-methyl-1-propene → Diethyl (2-methylprop-2-en-1-yl)(propan-2-yl)propanedioate
https://huagongshe.com/reaction/441841
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Diethyl isopropylmalonate | HCID 12966 | — |
| Reactant | Hexamethylphosphorous triamide | HCID 15355 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | HMPT toluene | HCID 131710867 | — |
| Product | Diethyl (2-methylprop-2-en-1-yl)(propan-2-yl)propanedioate | HCID 54297538 | — |
Reaction Steps
A solution of diethyl isopropylmalonate (8.1g) in 25 ml of a 25% solution of HMPT (hexamethylphosphorus triamide) in toluene was added dropwise over 15 minutes to a suspension of sodium hydride (50 mM) in 25% HMPT/toluene (50 ml) at room temperature. The mixture was then stirred at 60° C. for 1/2 hour, cooled to 25° C. and methallyl chloride (4.0g) in 25% HMPT/toluene was added over 10 minutes. The mixture was stirred at 80°-85° C. overnight, cooled to room temperature and poured onto a mixture of ice/hydrochloric acid. The product was extracted with ether, the ethereal extracts washed with water, followed by 2N sodium hydroxide and then water, and dried over magnesium sulphate. Removal of solvent gave diethyl isopropyl-2-methylprop-2-enylmalonate as a pale yellow liquid. R.I. nD21 1.4467.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04042710 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-e4fab342618b4a428769a1d589c27839 |
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| Source note | uspto-grants-1977_08 |
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