HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254436Generated: October 30, 2026
4-Toluenesulfonyl chloride → N-(2,2-Dimethoxy-ethyl)4-methyl-N-(5-methyl-thiophen-2-ylmethyl)-benzenesulfonamide
https://huagongshe.com/reaction/254436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2,2-Dimethyloxy-ethyl)-(5-methyl-thiophen-2-ylmethyl)-amine | HCID 14788182 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2,2-Dimethoxy-ethyl)4-methyl-N-(5-methyl-thiophen-2-ylmethyl)-benzenesulfonamide | HCID 66859761 | — |
Reaction Steps
Crude (2,2-dimethyloxy-ethyl)-(5-methyl-thiophen-2-ylmethyl)-amine (1) (43.41 g ˜75% pure, 0.15 mol) was dissolved in EtOAc (150 mL) resulting in a yellow solution. Triethylamine (22 mL, 0.16 mol) was added. The mixture was cooled to 0° C. in ice bath. p-Toluenesulfonyl chloride (29.68 g, 0.16 mol) was added in small portions keeping the temperature below 15° C. After addition was complete the mixture was left in ice bath and allowed to slowly warm to room temperature and stirred for 20 hrs. The milky-yellow mixture was diluted with EtOAc (300 mL) and washed with water (2×400 mL), 1 M HCl (2×400 mL), water (1×400 mL), sat NaHCO3 (1×400 mL), and brine (1×400 mL), dried (MgSO4) and condensed to provide the title compound as a reddish-yellow liquid, 50.56 g. Product was not purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07875627B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-9ee59b2efec0401d99b822c76a4adfbf |
|---|
| Source note | uspto-grants-2011_01 |
|---|