HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73427Generated: October 25, 2026
Dimethyl malonate → Dimethyl 2-(2-bromoallyl)malonate
https://huagongshe.com/reaction/73427
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | 2,3-Dibromopropene | HCID 10552 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Dimethyl 2-(2-bromoallyl)malonate | HCID 11054093 | 65% |
Reaction Steps
To a suspension of sodium hydride (5.0 g, 125 mmol) in HMPA (50 ml, distilled from calcium hydride) was added a solution of dimethyl malonate (11.7 ml, 100 mmol) in HMPA (5 ml) at 0° C. under argon. The mixture was heated to 50° C. and stirred 1 hour. Following this the solution was again cooled to 0° C., and a solution of 2,3-dibromopropene (122 ml, 100 mmol) in HMPA (5 ml) was added to the reaction mixture. Next, the solution was warmed to 40° C. and stirred for 1 hour. The reaction mixture was quenched with aq. HCl (10%, 88 ml) and extracted with ether (3×45 ml). The organic fractions were collected, dried over MgSO−4, and the solvent was removed in vacuo. The crude oil was purified via silica gel chromatography (eluants: chloroform/hexane) to obtain the titled product as a colorless oil (16.3 g, 65%). 1H-NMR (300 MHz, CDCl3) δ 5.70 (d, J=1.8 Hz, 1H), 5.48 (d, J=1.8 Hz, 1H), 3.63 (t, J=7.5 Hz, 1H), 3.76 (s, 6H), 3.04 (d, J=7.5 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829052B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f24be6e91b274e9c8521af976070ebff |
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| Source note | uspto-grants-2014_09 |
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