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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284747Generated: November 1, 2026

Benzenamine, 3-ethynyl- → HCID 90052292, compound

https://huagongshe.com/reaction/2284747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-ethynyl-HCID 104682—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-(2-oxoethyl)carbamateHCID 4247255—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 90052292HCID 90052292—

Reaction Steps

To a solution of 3-ethynylaniline (100 mg) and N-Boc-2-aminoacetaldehyde (407 mg) in ethyl acetate (5 mL) and methylene chloride (5 mL), acetic acid (2 drops) and sodium triacetoxyborohydride (543 mg) were added at room temperature, and the mixture was stirred at the same temperature for 3 hours and 30 minutes. To the reaction mixture, N-Boc-2-aminoacetaldehyde (200 mg) and sodium triacetoxyborohydride (200 mg) were added at room temperature, and the mixture was stirred at the same temperature. To the reaction mixture, saturated aqueous sodium hydrogencarbonate and ethyl acetate were added. The organic layer was separated, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (eluent, 75% hexane/25% ethyl acetate) to obtain tert-butyl (2-((3-ethynylphenyl)amino)ethyl)carbamate (G27).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-397c137f7ad84925887a90874b73a51d
Source noteuspto-grants-2015_09