HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369302Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 86672631, compound
https://huagongshe.com/reaction/2369302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylamine Hydrochloride | HCID 10313079 | — |
| Reactant | HCID 86672629 | HCID 86672629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86672631 | HCID 86672631 | — |
Reaction Steps
0.82 mL (5.9 mmol) of triethylamine, 0.90 g (4.7 mmol) of p-toluenesulfonyl chloride, 38 mg (0.39 mmol) of trimethylamine hydrochloride was added to a solution of 1.0 g (3.9 mmol) of 5,9,13-trimethyltetradec-4-en-1-ol in dry methylene chloride (3 mL) at 0° C., sequentially. After being stirred for 1 hour at room temperature, 0.12 mL (1.0 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 (5,9,13-trimethyltetradec-4-enyl)tosylate as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703922B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-fc4530aea58444d6b5ba3d6a01528a71 |
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| Source note | uspto-grants-2014_04 |
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