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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303686Generated: October 26, 2026

Sodium hydride → 2-(Diethoxyphosphoryl)-3-cyclopropylproprionic acid 4-methoxybenzyl ester

https://huagongshe.com/reaction/2303686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Diethoxyphosphoryl)acetic acid para-methoxybenzyl esterHCID 54020927—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-(Diethoxyphosphoryl)-3-cyclopropylproprionic acid 4-methoxybenzyl esterHCID 5408410560.9%

Reaction Steps

To a suspension of 60% sodium hydride in mineral oil (0.840 g, 21.0 mmol) in DMF (100 mL) was added a solution of 2-(diethoxyphosphoryl)acetic acid para-methoxybenzyl ester (6.04 g, 19.1 mmol) from Step A in DMF (10 mL). The reaction mixture was stirred for 30 min at room temperature. Bromomethylcyclopropane (2.4 mL, 24.8 mmol) was added and the reaction mixture was stirred at rt for 12 h. The reaction mixture was diluted with diethyl ether, poured into saturated sodium bicarbonate, and extracted three times with diethyl ether. The organic layers were combined, washed with saturated sodium chloride, dried over sodium sulfate, and filtered. The volatiles were removed in vacuo and the residue was purified by FC (40% ethyl acetate in hexanes) to afford 4.31 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-5fbe0a5fb4fc4a60bad773b49e34a777
Source noteuspto-grants-2002_08