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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370318Generated: November 2, 2026

Triethylamine → HCID 54416712, compound

https://huagongshe.com/reaction/370318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Methylthio)benzaldehydeHCID 76985—
ReactantMagnesium BromideHCID 82241—
ReactantTriethyl 2-phosphonopropionateHCID 107155—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 54416712HCID 5441671295%

Reaction Steps

To a solution of triethyl 2-phosphonopropionate (47 g, 0.19 mol) in THF (200 mL) was added solid magnesium bromide etherate (59 g, 0.23 mol) under nitrogen. Triethylamine (26.5 mL, 0.19 mol) was added after 5 min. The mixture was stirred for 10 min and 4-(methylthio)benzaldehyde (27.1 mL, 0.19 mol) was added. After 15 h at room temperature the mixture was diluted with water (400 mL) and hexane (400 mL). The two layers were separated. The organic layer was washed with water (400 mL), dried over 4 Å molecular sieves, filtered, and concentrated to give 42.5 g (95%) of ester 6a as a light yellow oil: IR (neat) 2980, 1705, and 1240 cm-1 ; 1H NMR (CDCl3, 300 MHz) δ 7.63 (1 H), 7.33 (2 H), 7.25 (2 H), 4.26 (2 H), 2.50 (3 H), 2.12 (3 H), and 1.34 (3 H); 13C NMR (CDCl3, 75.5 MHz) δ 168.71, 139.37, 138.08, 132.55, 130.19, 127.98, 125.89, 60.87, 15.38, 14.37 and 14.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140515
Source datasetuspto-grants-2000_10
ORD IDord-11c045263ed64978a107e051f15eea11
Source noteuspto-grants-2000_10