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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227618Generated: October 31, 2026

Sodium Chloride → 3-(Propionylthio)-1-propyltrimethoxysilane

https://huagongshe.com/reaction/2227618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant(3-Mercaptopropyl)trimethoxysilaneHCID 20473—
ReactantPropionyl chlorideHCID 62324—
ReactantSodium MethoxideHCID 10942334—
Reactant3-(Acetylthio)-1-propyltrimethoxysilaneHCID 12135710—
ReactantTrimethoxy[3-(methylsulfanyl)propyl]silaneHCID 13307608—
SolventTolueneHCID 1140—
Product3-(Propionylthio)-1-propyltrimethoxysilaneHCID 12135711—

Reaction Conditions

Temperature32.5 °C

Reaction Steps

1035 grams of 3-mercapto-1-propyltrimethoxysilane, 1096 grams of a 25 weight percent methanolic solution of sodium methoxide, and 1764 grams of toluene were charged to a 5-liter flask under an atmosphere of nitrogen. The stirred mixture developed a pinkish color. The flask was placed into a water bath at 64° C. Methanol was removed from the flask by distilling off a methanol-toluene azeotrope under a partial vacuum. The vacuum was kept such that the temperature in the distillation head was maintained at 30 to 35° C. during which time 1500 ml of distillate, consisting of a toluene-methanol azeotrope, was collected. During this time the contents of the flask turned colorless. An additional 429 grams of toluene was added and the distillation resumed. The appearance of a strong density current in the distillate which coincided with an increase in distillation head temperature from 35 to 55° C. and the appearance of a changing liquid surface tension in the condenser signaled the point at which methanol removal from the flask was complete. The contents of the flask had become a viscous fluid. With continued stirring, the contents of the flask were allowed to cool. The flask was placed in an ice-water bath resulting in what appeared to be a thick paste. 457 grams of propionyl chloride was added to the flask drop-wise and/or in small portions with continued stirring in an ice-water bath until the reaction was complete. Aliquots of the stirred mixture were taken periodically. An alkaline reading indicated the completion of the reaction. The final mixture was a white suspension of NaCl in a toluene solution of the product. This mixture was filtered and the solvent was removed from the filtrate to yield a nearly colorless product. Gas chromatography indicated (by weight) 3 percent of 3-mercapto-1-propyltrimethoxysilanec, 1 percent of 3-(methylthio)-1-propyltrimethoxysilane, and 96 percent of 3-(acetylthio)-1-propyltrimethoxysilane (product). Flash distillation from 1 to 2 grams of powdered sodium methoxide yielded a colorless product. The sodium methoxide was added to ensure that any remaining acidity was neutralized. Further optional fractional distillation yielded a product in excess of 98 percent purity by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414061B1
Source datasetuspto-grants-2002_07
ORD IDord-fd4db197d5a642f5827683c7232f4eba
Source noteuspto-grants-2002_07