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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910362Generated: November 1, 2026

Water → HCID 131731068, compound

https://huagongshe.com/reaction/1910362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSalicyl AlcoholHCID 5146—
ReactantSilane, dichloromethyloctadecyl-HCID 78835—
ReactantDiisopropylethylamineHCID 81531—
SolventTolueneHCID 1140—
ProductHCID 131731068HCID 131731068—

Reaction Conditions

Temperature40 °C

Reaction Steps

In a 1 l four-neck flask with stirrer, reflux condenser and dropping funnel, 31.7 g of salicyl alcohol (0.25 mol) and 66.7 g (0.52 mol) of dried N-ethyldiisopropylamine were suspended under argon in 100 ml of anhydrous toluene at 22° C. 110 g of Octadecylmethyldichlorosilane (95%; 0.25 mol) was melted and dissolved in 100 ml of dry toluene. This solution was added dropwise at 23 to 27° C. within 55 minutes, in the course of which an exothermic reaction was observed. Cooling with an ice bath held the reaction temperature at a maximum of 27° C. After the addition had ended, the temperature was raised to 40° C., and exothermicity (without heating to 45° C.) was again observed. The reaction vessel was then cooled to 40° C. with cold water, and it was stirred at this temperature for one hour and then cooled to RT. The suspension was left to stand at RT overnight. The precipitate (hydrochloride) was filtered off with suction through a P40 glass frit under N2, and the filtrate was concentrated by rotary evaporation at 120° C./5 mbar. Yield 80.9 g (77% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08603681B2
Source datasetuspto-grants-2013_12
ORD IDord-3f107be11d5d46d38fdf666f3daf389e
Source noteuspto-grants-2013_12