Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369289Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 86672628, compound

https://huagongshe.com/reaction/2369289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantTriethylamineHCID 8471—
ReactantTrimethylamine HydrochlorideHCID 10313079—
ReactantHCID 86672627HCID 86672627—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86672628HCID 86672628—

Reaction Steps

0.49 mL (3.5 mmol) of triethylamine, 0.68 g (3.54 mmol) of p-toluenesulfonyl chloride, 15 mg (0.16 mmol) of trimethylamine hydrochloride were added to a solution of 1.0 g (3.2 mmol) of 4,8,12,16-tetramethylheptadec-3-en-1-ol in dry methylene chloride (3.2 mL) at 0° C., sequentially. After being stirred for 2 hours at room temperature, 0.080 mL (0.64 mmol) of N,N-dimethyl-1,3-propanediamine was added to the reaction mixture at 0° C. After being stirred for 15 min, water was added, and the mixture was extracted with methylene chloride. The extract was washed with 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 (4,8,12,16-tetramethylheptadec-3-enyl)tosylate as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703922B2
Source datasetuspto-grants-2014_04
ORD IDord-21cc80e40bb247b187d592f762691a5b
Source noteuspto-grants-2014_04