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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273257Generated: November 1, 2026

Acetic Acid → HCID 86671547, compound

https://huagongshe.com/reaction/2273257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
ReactantTriethylamineHCID 8471—
ReactantDiazomethaneHCID 9550—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 67247248HCID 67247248—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86671547HCID 8667154725%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (110 μL, 0.77 mmol, 2.0 eq) is added at 0° C. to a stirred solution of 6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthrene-3-carboxylic acid (100 mg, 0.39 mmol, 1.0 eq) in tetrahydrofuran (10 mL), followed by ethyl chloroformate (73 μL, 0.77 mmol, 2.0 eq). After 1 hour stirring at 0° C., a solution of diazomethane in diethyl ether (20 mL, freshly prepared) is added at 0° C. to the reaction mixture. After 2 hours stirring at 0° C., a 33% hydrobromic acid solution in acetic acid (200 μL, 1.16 mmol, 3.0 eq) is added at 0° C. to the reaction mixture. After 1 hour stirring at 0° C., solvent is removed to give a crude product that is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 3:1, v/v) to afford 2-bromo-1-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-yl)-ethanone as a light yellow oil (33 mg, 25% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120822B2
Source datasetuspto-grants-2015_09
ORD IDord-e38c7b0067c44221ac26fdd5a678bbf9
Source noteuspto-grants-2015_09