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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458941Generated: October 29, 2026

Ethyl bromoacetate → HCID 18442436, compound

https://huagongshe.com/reaction/458941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18442437HCID 18442437—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
ProductHCID 18442436HCID 1844243689%

Reaction Conditions

Temperature60 °C

Reaction Steps

1,1-Dioxo-3,3-dibutyl-5-(4-t-butoxycarbonylaminophenyl)-8-hydroxy-2,3,4,5-tetrahydro-1,5-benzothiazepine Method 107; 597 mg, 1.16 mmol) was dissolved in MeCN (20 ml), K2CO3 (480 mg, 3.5 mmol), tetrabutylammoniumbromide (54 mg, 0.17 mmol) and ethyl bromoacetate (167 μl, 1.5 mmol) was added. The mixture was heated to 60° C. overnight. The solvent was evaporated under reduced pressure. EtOAc and water was added and the water layer was extracted two times with EtOAc. The combined organic layer was washed once with brine, dried, filtered and evaporated under reduced pressure to give the title compound 0.617 g (89%). M/z 603.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192945B2
Source datasetuspto-grants-2007_03
ORD IDord-42ced3ead2c6485f9a367f3cd04ef03e
Source noteuspto-grants-2007_03