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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369312Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 86672634, compound

https://huagongshe.com/reaction/2369312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantTriethylamineHCID 8471—
ReactantTrimethylamine HydrochlorideHCID 10313079—
ReactantHCID 86672633HCID 86672633—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86672634HCID 86672634—

Reaction Steps

0.63 mL (4.6 mmol) of triethylamine, 0.87 g (4.6 mmol) of p-toluenesulfonyl chloride, and 20 mg (0.21 mmol) of trimethylamine hydrochloride were added to a solution of 1.0 g (4.2 mmol) of 4,8,12-trimethyltridec-3-en-1-ol in dry methylene chloride (3 mL) at 0° C., sequentially. After being stirred for 2 hours at room temperature, 0.10 mL (0.83 mmol) of N,N-dimethyl-1,3-propanediamine was added to the reaction mixture at 0° C. After being stirred for 30 min, 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 (4,8,12-trimethyltridec-3-enyl)tosylate as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703922B2
Source datasetuspto-grants-2014_04
ORD IDord-dde91abc788744e287aceed227cc6a04
Source noteuspto-grants-2014_04