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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84097Generated: October 29, 2026

Diiodomethane → N-Trifluoroacetyl-1-cyclopropyl-7-ethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/84097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-Trifluoroacetyl-7-methoxy-1-methylene 2,3,4,5-tetrahydro-1H-3-benzazepineHCID 22292788—
ReactantHCID 178418750HCID 178418750—
SolventDichloromethaneHCID 6344—
ProductN-Trifluoroacetyl-1-cyclopropyl-7-ethoxy-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 86692803—

Reaction Steps

A solution of diethyl zinc (1 mL, 1M in hexanes) in dichloromethane (1 mL) at 0 C was treated with trifluoroacetic acid in dichloromethane (0.5 mL) and the mixture stirred for 15 min. Diiodomethane (0.280 g, 1.0 mmol) in dichloromethane (0.5 mL) was then added and stirred for 15 minutes. N-Trifluoroacetyl-7-methoxy-1-methylene-2,3,4,5-tetrahydro-1H-3-benzazepine (0.075 g, 0.26 mmol) in dichloromethane (1 mL) was added and the mixture stirred for 30 minutes at 0 C and then for 2 hours at 20 C. The product mixture was quenched with aqueous saturated NH4Cl (5 mL), extracted twice with CH2Cl2 (20 mL), washed with saturated aqueous NaHCO3 (10 mL), washed with H2O (10 mL), and concentrated. Flash chromatography (7% EtOAc in hexanes, silica) resulted in 0.050 g of a white solid. MS calculated for C15H16F3NO2+H: 300, observed: 300.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846906B2
Source datasetuspto-grants-2014_09
ORD IDord-a2a5259243f84507ad3518c5187adba6
Source noteuspto-grants-2014_09