HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577724Generated: November 1, 2026
4-Toluenesulfonyl chloride → HCID 86679665, compound
https://huagongshe.com/reaction/577724
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Dimethylamino)-1,2-propanediol | HCID 79078 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86679665 | HCID 86679665 | — |
Reaction Steps
To a solution of 3-(dimethylamino)propane-1,2-diol (934 mg, 7.84 mmol) in CH2Cl2 (8 mL) were added Bu2SnO (42 mg, 0.16 mmol), tosyl chloride (1.49 g, 7.84 mmol), and Et3N (1.10 mL, 7.92 mmol). The reaction mixture was stirred at rt for 2 hrs. The mixture was quenched with water (30 mL) and extracted with EtOAc (two×30 mL). The combined organic layers were dried over MgSO4 and concentrated to afford 3-dimethylamino-2-hydroxypropyl 4-methylbenzenesulfonate; [m/z (APCI+) 274.10 (M+H)+]. The residue was dissolved in THF (10 mL), then DBU (2.56 mL, 16.6 mmol) and 4-nitro-1H-pyrazole (602 mg, 5.32 mmol) were added and the resulting mixture was stirred at rt for 30 min. The mixture was then quenched with water (30 mL) and extracted with EtOAc (two×30 mL). The combined organic layer were dried over MgSO4 and concentrated to give the title compound as a pale yellow oil (526 mg, 46° A yield) which was used without purification. m/z (APCI+) for C8H14N4O3 215.10 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040547B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-26bedb0bfd5a4f8a83ac05ca71b909ad |
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| Source note | uspto-grants-2015_05 |
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