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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
Reactantethyl 2-hydroxypent-4-enoateHCID 10986362—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Methyl-allyloxy)-pent-4-enoic acid ethyl esterHCID 5975234566%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357718B2
Source datasetuspto-grants-2013_01
ORD IDord-3980e6e15dec443680c99ed38b5a74b0
Source noteuspto-grants-2013_01