HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261385Generated: November 1, 2026
4-Toluenesulfonyl chloride → 3-(4-Methylphenyl)propyl 4-methylbenzene-1-sulfonate
https://huagongshe.com/reaction/2261385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(4-Methylphenyl)propan-1-ol | HCID 221893 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Methylphenyl)propyl 4-methylbenzene-1-sulfonate | HCID 53903301 | 70% |
Reaction Steps
2.46 g of tosyl chloride (13 mmol), 3.4 ml of diisopropylamine (19.4 mmol) and 158 mg of 4-(dimethylamino)pyridine (1.29 mmol) were added to reaction solution (6.46 mmol) dissolving 971 mg of 3-p-tolyl-propane-1-ol (40ac) prepared by above step 3 in methylene chloride at 0° C. under Ar atmosphere with stirring for 6 hrs, and the reaction mixture was stirred for 12 hrs at room temperature. After the reaction mixture was neutralized with ammonium chloride, the mixture was extracted with ethyl acetate, washed with saturated NaCl solution, dried over MgSO4, filtered, and concentrated in vacuo. The resultant was purified by Silica gel column chromatography with a solvent mixture mixed with methanol and chloroform (1:7) as an eluant to give 1.3 g of toluene-4-sulfonate-3-p-tolyl-propyl ester (40ad) (yield: 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846963B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-f9604a9b264340b29eef9cb8e98b7028 |
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| Source note | uspto-grants-2010_12 |
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