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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184068Generated: October 31, 2026

HCID 4232364, compound → 3-(Trimethylsilyl)propane-1-sulfonic acid

https://huagongshe.com/reaction/2184068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 4232364HCID 4232364—
ReactantSodium 3-(trimethylsilyl)-1-propanesulfonateHCID 5167273—
SolventWaterHCID 962—
Product3-(Trimethylsilyl)propane-1-sulfonic acidHCID 74873—

Reaction Steps

A solution of sodium 3-(trimethylsilyl)-1-propanesulfonate (9 grams, 41.2 mmol) dissolved in demineralized water (75 ml) was added drop wise into a short column packed with an excess (15-20 times the molar amount of 3-(trimethylsilyl)-1-propanesulfonate) of Tulsion T-42 MP(H+) acidic ion exchange resin. Then the resin bed was washed with water until the pH of the solution eluting from the column was about 5 to 6. The water solution of the free 3-(trimethylsilyl)-1-propanesulfonic acid thus obtained was neutralized with tetra-n-butylammonium hydroxide until the pH of the solution was about 5 to 5.5. The resulting mixture was extracted with chloroform (three times) and the combined chloroform washes was washed with water (three times). The chloroform layer was separated, dried with anhydrous sodium sulfate, and concentrated under reduced pressure to remove solvent and other volatiles. The residual material was finally dried at 40° C. and 0.1 mm Hg to afford tetra-n-butylammonium 3-(trimethylsilyl)-1-propanesulfonate as a hygroscopic white solid. The yield of the product was 17.4 grams, or 97% of the theoretical amount. Proton NMR spectrum of the compound indicated that it was the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900257B2
Source datasetuspto-grants-2005_05
ORD IDord-5c247059d4f94d9aabee178391990264
Source noteuspto-grants-2005_05