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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930804Generated: October 28, 2026

Ethyl bromoacetate → HCID 90303921, compound

https://huagongshe.com/reaction/930804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant3,4-Difluorobenzyl alcoholHCID 522833—
Reactant8-Chloro-3,4-dihydro-1H-pyrimido[1,6-A]pyrimidin-6(2H)-oneHCID 135741882—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90303921HCID 9030392132.8%

Reaction Steps

To a solution of 8-chloro-3,4-dihydro-1H-pyrimido[1,6-a]pyrimidin-6(2H)-one (5 g, 26.9 mmol) in tetrahydrofuran (20 mL) was added sodium hydride (2.59 g, 108 mmol) at r.t. stirred for 10 minutes at r.t., then was added ethyl 2-bromoacetate (4.50 g, 26.9 mmol) and stirred for 2 h, and followed by addition of (3,4-difluoro phenyl)methanol (3.88 g, 26.9 mmol). The reaction mixture was stirred for 1 h at r.t., quenched by addition of water, and extracted by EtOAc. The aqueous phase was acidified to pH˜1 with HCl (1N), washed by EtOAc, then the aqueous phase was concentrated in vacuum, and the residual was washed by methanol and filtrated. The filtrate was concentrated to afford the title compound (3.1 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296755B2
Source datasetuspto-grants-2016_03
ORD IDord-3300dc6f5b964b05ab7ea71dd6f1a9a9
Source noteuspto-grants-2016_03