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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905014Generated: October 29, 2026

4-Toluenesulfonyl chloride → HCID 13189250, compound

https://huagongshe.com/reaction/905014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-(1-Ethoxyethoxy)-3,3-difluoro-4-methylpentan-1-olHCID 13189249—
SolventPyridineHCID 1049—
ProductHCID 13189250HCID 13189250—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1.00 g (0.0044 mol) of 4-(1-ethoxyethoxy)-3,3-difluoro-4-methyl-1-pentanol, 4 mL of pyridine and 1.27 g (0.0066 mol) of p-toluenesulfonyl chloride was stirred at 0° C. for 18 hr. The mixture was quenched with ice chips. The mixture was then poured into water and extracted with methylene chloride. The organic phase was sequentially washed with 10% aqueous sulfuric acid and saturated aqueous sodium bicarbonate solution. The organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to yield oily 4-(1-ethoxyethoxy)-3,3-difluoro-4-methyl-1-pentanol 1-(4-methylbenzenesulfonate). NMR (CDCl3) δ4.93 (quartet, 1, J=7 Hz), 4.27 (triplet, 2, J=7 Hz), 3.45 (quartet, 2, J=7 Hz), 2.45 (singlet, 3), 2.36 (multiplet, 2), 1.27 (triplet, 6, J=1 Hz), 1.24 (doublet, 3 J=7 Hz), and 1.15 ppm (triplet, 3, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04421690
Source datasetuspto-grants-1983_12
ORD IDord-6b61fc97dba0463bb493461cb9053360
Source noteuspto-grants-1983_12