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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380643Generated: October 31, 2026

Ethyl bromoacetate → HCID 11027636, compound

https://huagongshe.com/reaction/380643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 11091194HCID 11091194—
SolventDimethylformamideHCID 6228—
ProductHCID 11027636HCID 11027636—

Reaction Steps

To a mixture of (2R)-2-{[N,N-di(4-fluorophenyl)-carbamoyloxy]methyl}-2,5-dihydroxy-1,2,3,4-tetrahydro-naphthalene (0.18 g) and powder K2CO3 in dry DMF (1.8 ml) was added ethyl bromoacetate (0.047 ml) at room temperature. After stirring for 16 hours, the reaction mixture was partitioned between AcOEt and water. The organic layer was washed with water, brine, dried over MgSO4 and evaporated in vacuo. The residue was crystallized from n-hexane to give (2R)-2-{[N,N-di(4-flurophenyl)carbamoyloxy]methyl}-5-[(ethoxycarbonyl)methoxy]-2-hydroxy-1,2,3,4-tetrahydronaphthalene (0.16 g) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303649B1
Source datasetuspto-grants-2001_10
ORD IDord-12ef946b3a2e4a149cc74b710c04601c
Source noteuspto-grants-2001_10