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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404348Generated: October 31, 2026

Ethyl bromoacetate → HCID 178525872, compound

https://huagongshe.com/reaction/1404348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178511528HCID 178511528—
SolventMethanolHCID 887—
ProductHCID 178525872HCID 178525872—

Reaction Steps

To (R)-3-(2-(trans-4-aminocyclohexyl)acetamido)-2-hydroxy-3,4-dihydro-2H-benzo[e][1,2]oxaborinine-8-carboxylic acid (Example 6) in MeOH was added TEA (2.5 eq), followed by ethyl bromoacetate (1.2 eq). The reaction mixture was stirred at RT overnight. To this reaction mixture was then added 1N NaOH and stirred for 6 hr. After concentration in vacuo, 1N HCl was added to adjust pH to 1. The reaction mixture was purified using reverse phase HPLC to afford the title compound. ESI-MS m/z 405 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912169B2
Source datasetuspto-grants-2014_12
ORD IDord-219bf9fb704c4e4caca3e902c4431db8
Source noteuspto-grants-2014_12