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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463431Generated: November 2, 2026

Triethylamine → HCID 19018149, compound

https://huagongshe.com/reaction/1463431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyanogen BromideHCID 10476—
ReactantHCID 22111943HCID 22111943—
SolventDichloromethaneHCID 6344—
ProductHCID 19018149HCID 1901814999.4%

Reaction Steps

To a 750 ml methylene chloride solution containing 40.2 g (0.1 mole) of 1,3-bis-(3'-(2-hydroxylphenyl)-propyl)-1,1,3,3-tetramethyldisiloxane from A above is added 25.42 g (0.24 mole, 97% purity) of cyanogen bromide (CNBr) at -30° C. and 26.31 g (0.26 mole, 98% purity) of triethylamine is then added at -30° C. in 15 minutes. An exothermic reaction is observed. After completion of addition, the reaction temperature is maintained at -25° C. to -15° C. for 30 minutes and -15° C. to -5° C. for 30 min. The mixture is then hydrolyzed with 150 ml H2O and washed once with 0.2N HCl and three times with 150 ml portions of H2O. The solution is dried over MgSO4, resulting in 45 g of a viscous liquid after stripping off solvent at <145° C./<10 mm Hg. The structure is confirmed by IR and 1H NMR. IR(neat): 3350 cm-1 (aromatic hydroxyl disappeared), 2250 cm-1 (strong --CN); 1H NMR (CDCl3): 0 to 0.8 ppm (m, Si--CH3 and Si--CH2 --), 1.6-2.0 ppm (m, --CH2 --), 2.8 ppm (t, --CH2 --), 7.3-7.6 ppm (m, Ar--H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300591
Source datasetuspto-grants-1994_04
ORD IDord-28b469a1a46e47eea6227e48f98ebd5b
Source noteuspto-grants-1994_04