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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921465Generated: October 31, 2026

Benzylamine → HCID 68156973, compound

https://huagongshe.com/reaction/921465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantEthylamine hydrochlorideHCID 11198—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58071501HCID 58071501—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68156973HCID 6815697346.1%

Reaction Conditions

Temperature105 °C

Reaction Steps

Diethenyl(3-methoxy-4-nitrophenyl)phosphane oxide (0.480 g, 1.94 mmol), ethylamine hydrochloride (0.174 g, 2.12 mmol), and 1 N NaOH (2 mL) were dissolved in 50% aqueous THF (5 mL) and heated to 105° C. under nitrogen. After one hour, another portion of benzylamine was added to the reaction mixture. The reaction mixture was refluxed for an additional 2 h, and then cooled to room temperature. The reaction mixture was partitioned between saturated aqueous NaHCO3 and CH2Cl2. The aqueous phase was washed once with CH2Cl2 and the organic layers were combined. The organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel chromatography (0-10% 7N ammonia in methanol:dichloromethane) to afford the compound (0.267 g, 46% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273077B2
Source datasetuspto-grants-2016_03
ORD IDord-a8d7d00a705c4d50b2d905e7d6d656fe
Source noteuspto-grants-2016_03