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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372536Generated: November 1, 2026

Ethyl Acetate → HCID 9835084, compound

https://huagongshe.com/reaction/1372536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantHCID 9966834HCID 9966834—
ReactantHCID 178418546HCID 178418546—
SolventWaterHCID 962—
ProductHCID 9835084HCID 983508459.7%

Reaction Steps

A mixture of crude 7-amino-8-bromo-9a-ethyl-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (0.97 g, 3.02 mmol), CuCN (0.318 g, 3.55 mmol), and 1-methyl-2-pyrrolidinone (NMP, 6 mL) was placed under a N2 atmosphere, stirred, and heated in an oil bath at 160–170° C. for 5.5 hours. After cooling to room temperature, the mixture was added to EtOAc (200 mL) and water (200 mL) and filtered through a pad of solka-floc. The organic portion of the filtrate was washed with water (5×200 mL) and brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to a red oil (0.8 g). The crude product was purified by chromatography on EM silica gel 60 (2.75×25 cm column), eluting with 5% EtOAc in CH2Cl2, to afford 7-amino-8-cyano-9a-ethyl-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (0.48 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157604B2
Source datasetuspto-grants-2007_01
ORD IDord-a367a408430944bbb08399596fe2ba10
Source noteuspto-grants-2007_01