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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628341Generated: October 31, 2026

Ethyl bromoacetate → HCID 67496386, compound

https://huagongshe.com/reaction/1628341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67497334HCID 67497334—
SolventDimethylformamideHCID 6228—
ProductHCID 67496386HCID 6749638649%

Reaction Conditions

Temperature0 °C

Reaction Steps

103.1.B (905 mg, 2.65 mmole), 5 ml of DMF and 0.69 ml of DIEA. The reaction mixture was cooled to 0° C., and then ethyl bromoacetate (0.49 g, 2.92 mmole) was added to the mixture. The reaction was stirred at room temperature overnight. After then, the solution was poured into saturated ammonium chloride, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. After concentration in vacuo, the residue was chromatographed on silica gel to give 103.1.C (552 mg, 49% yield) as orange syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785468B2
Source datasetuspto-grants-2014_07
ORD IDord-ef2d8949056740e0a47fde76d6e005a8
Source noteuspto-grants-2014_07