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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458943Generated: October 30, 2026

Ethyl bromoacetate → HCID 18442441, compound

https://huagongshe.com/reaction/458943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 18442442HCID 18442442—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
ProductHCID 18442441HCID 18442441106.8%

Reaction Steps

To a suspension of 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-hydroxy-2,3,4,5-tetrahydro-1,5-benzothiazepine (Method 26; 12.85 g, 28.71 mmol) in MeCN (150 ml) was added ethyl bromoacetate (3.85 ml, 34.6 mmol), tetrabutylammonium bromide (0.925 g, 2.869 mmol) and sodium carbonate (12.85 g, 121.2 mmol). The mixture was heated under reflux for 5 hours. The solvent was removed under reduced pressure and the residue was partitioned between DCM and 0.5 M HCl. The organic layer was washed with brine, dried (MgSO4) and concentrated. Chromatography using DCM/EtOAc (9:1) as eluent gave the desired product (15.45 g) as a tan oil. NMR 0.70–0.85 (m, 6H), 1.00–1.55 (m, 15H), 2.15 (s, 3H), 3.10 (s, 2H), 3.70 (bs, 2H), 4.25 (q, 2H), 4.70 (s, 2H), 6.65 (s, 1H), 6.90–7.30 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192945B2
Source datasetuspto-grants-2007_03
ORD IDord-6145cec9f7184ce68059aa596fdd56e7
Source noteuspto-grants-2007_03