HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113733Generated: October 29, 2026
Pentane → 5-Diallylaminomethyl-thiophene-2-sulfonyl chloride
https://huagongshe.com/reaction/2113733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | N-[(5-{[2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino}butanoyl)hydrazino]sulfonyl}thien-2-yl)methyl]-4-nitrobenzamide | HCID 9895318 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Diallylaminomethyl-thiophene-2-sulfonyl chloride | HCID 11380769 | 53% |
Reaction Steps
A solution of the allyl-protected thiophene 19a (6.2 g, 32.1 mmol) in Et2O was cooled to −70° C. by means of an acetone/dry ice bath. A solution of t-BuLi in pentane (21.38 ml, 1.5M, 32.1 mmol) was added over 2 min whereupon the internal temperature momentarily rose to −50° C. and the mixture turned orange. After 10 min., SO2 was bubbled for 2 min, which led to the immediate formation of a thick precipitate. The reaction was allowed to reach 0° C., and a suspension of NCS (4.63 g, 32.1 mmol) in THF (20 ml) was added, whereupon the slurry turned purple. After 45 min at r.t., the mixture was filtered over SiO2, eluting with EtOAc. Evaporation, dilution with EtOAc:hexane 1:5 and filtration over SiO2 gave 5.0 g (53%) of the title sulfonyl chloride 19b as a pale brown oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07432286B1 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-0a46cfb1cc904262b085e15aa3a734f5 |
|---|
| Source note | uspto-grants-2008_10 |
|---|