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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071308Generated: October 30, 2026

Ethyl bromoacetate → HCID 22393120, compound

https://huagongshe.com/reaction/1071308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 22393106HCID 22393106—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
ProductHCID 22393120HCID 2239312098.9%

Reaction Steps

1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methoxy-8-hydroxy-2,3,4,5-tetrahydro-1,5-benzothiazepine (WO 9616051; 1.0 g), ethyl bromoacetate (0,50 g), sodium carbonate (1.2 g) and tetrabutylammonium bromide (60 mg) in MeCN (15 ml) were refluxed over night. The solvent was removed under reduced pressure and the residue was extracted (DCM/H2O). The organic layer was separated and the solvent was removed under reduced pressure. The residue purified by chromatography (DCM/EtOAc (90:10)) to give the title compound 1.2 g (98%). NMR (400 MHz, CD3OD) 0.75-0.85 (m, 6H), 1.00-1.30 (m, 8H), 1.35-1.55 (m, 4H), 3.20 (s, 2H), 3.65 (s, 3H), 3.70 (brs, 2H), 4.50 (s, 2H), 6.50 (s, 1H), 6.90-7.30 (m,5H), 7.40 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906058B2
Source datasetuspto-grants-2005_06
ORD IDord-8334473c334346578a9854a53a46afeb
Source noteuspto-grants-2005_06