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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445306Generated: October 31, 2026

Ethyl formate → Ethyl 2-[(2H-1,3-benzodioxol-5-yl)methyl]-3-oxopropanoate

https://huagongshe.com/reaction/1445306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 1,3-benzodioxole-5-propionateHCID 81545—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[(2H-1,3-benzodioxol-5-yl)methyl]-3-oxopropanoateHCID 10060648—

Reaction Steps

First, 42.4 g of 60% NaH was suspended in 500 ml of tetrahydrofuran (THF). 84.5 g (purity: 93.7% by weight) of ethyl 3-(3,4-methylenedioxyphenyl)-propionate was dissolved in 100 ml of THF and added dropwise to the suspension solution prepared above at room temperature. After the resultant suspension solution was raised in temperature to 40° C. and stirred for 15 minutes, 131 g of ethyl formate was added dropwise for 2.5 hours to the suspension solution and stirred for a further 3 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666659B2
Source datasetuspto-grants-2010_02
ORD IDord-98f38d7cc9aa4ea591aa80a17b083bf6
Source noteuspto-grants-2010_02