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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709754Generated: October 30, 2026

1,5-Pentanediol → HCID 54485748, compound

https://huagongshe.com/reaction/1709754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-PentanediolHCID 8105—
ReactantTriethylamineHCID 8471—
ReactantMethanedisulphonyl dichlorideHCID 79863—
Reactant1,1-Ethanedisulfonyl chlorideHCID 23036726—
ReactantHCID 86744169HCID 86744169—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 54485748HCID 54485748—

Reaction Steps

1,5-Pentanediol (4.17 g, 0.04 mole) was dissolved in 350 ml of glyme in a 1 liter round bottom flask and the solution brought to -20° C. 1,1-ethanedisulfonyl chloride, synthesized in the same manner as the methanedisulfonyl chloride, (Example I) was dissolved in 25 ml of glyme and this solution added dropwise to the solution in the flask. Triethylamine (8.08 g, 0.08 mole) was dissolved in 125 ml of glyme and this solution was added to the pentanediol/ ethanedisulfonyl chloride solution over a 1 hour period. After the additions were completed, the mixture was brought to 25° C. over a 45 minute period in a water bath. The mixture was roto-evaporated under reduced pressure, at a temperature below 35° C. The residue was washed three times with 20 ml of 5% sodium bicarbonate the resulting emulsion being separated by centrifugation. Water was decanted from the final oil wash, and methylene chloride was added. This solvent apparently dissolved all or most of the impurities, leaving the product suspended in the solution. The product was obtained by vacuum filtering the solution through Whatman #5 qualitative filter papers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950768
Source datasetuspto-grants-1990_08
ORD IDord-008355b9185e401f92e625554c7ddcba
Source noteuspto-grants-1990_08