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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369280Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 86672618, compound

https://huagongshe.com/reaction/2369280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantTriethylamineHCID 8471—
ReactantTrimethylamine HydrochlorideHCID 10313079—
ReactantHCID 86672617HCID 86672617—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86672618HCID 86672618—

Reaction Steps

1.28 mL (9.23 mmol) of triethylamine, 1.06 g (5.56 mmol) of p-toluenesulfonyl chloride, 43 mg (0.45 mmol) of trimethylamine hydrochloride were added to a solution of 1.50 g (4.63 mmol) of 5,9,13,17-tetramethyloctadec-4-en-1-ol in dry methylene chloride (9 mL) was added, at 0° C., sequentially. After being stirred for 3 hours at room temperature, 0.14 mL (1.1 mmol) of N,N-dimethyl-1,3-propanediamine was added to the reaction mixture at 0° C. After being stirred for 3 hours, the mixture was diluted with ethyl acetate. The resulting solution was washed with water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous solution, and saturated brine, successively, and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated to obtain (5,9,13,17-tetramethyloctadec-4-enyl)tosylate as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703922B2
Source datasetuspto-grants-2014_04
ORD IDord-32f1db7861c04628a20b852b3eb47773
Source noteuspto-grants-2014_04