HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808004Generated: October 31, 2026
Sodium hydride → 2-(2-Methyl-allyloxy)-pent-4-enoic acid ethyl ester
https://huagongshe.com/reaction/1808004
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Reactant | ethyl 2-hydroxypent-4-enoate | HCID 10986362 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Methyl-allyloxy)-pent-4-enoic acid ethyl ester | HCID 59752345 | 66% |
Reaction Steps
To a cold (0° C.) stirred suspension of NaH (55% dispersion in oil, 227.9 mg, 5.2 mmol, 1.3 eq) in THF (20 mL) was added drop wise a solution of 2-hydroxy-pent-4-enoic acid ethyl ester (0.576 g, 4.0 mmol) in THF (20 mL) and stirred for 1 h. The reaction mixture was then treated with 3-bromo-2-methylpropene (0.81 g, 6.0 mmol, 0.61 mL), slowly warmed up to rt, and stirred for 1 h. It was carefully quenched with saturated NH4Cl solution. Reaction mixture was extracted with EtOAc (3×20 mL) organic solution was washed with brine, dried (Na2SO4), concentrated. Purification of the residue on silica gel column chromatography using 5% EtOAc-Hexane furnished 2-(2-methyl-allyloxy)-pent-4-enoic acid ethyl ester (0.521 g, 66%) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357718B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-3980e6e15dec443680c99ed38b5a74b0 |
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| Source note | uspto-grants-2013_01 |
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