HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369309Generated: October 31, 2026
4-Toluenesulfonyl chloride → HCID 86672634, compound
https://huagongshe.com/reaction/2369309
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 86672633 | HCID 86672633 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86672634 | HCID 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 then 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
| 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-3ab23e48ac2441e794f49a57fa462572 |
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| Source note | uspto-grants-2014_04 |
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