HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → 2-[(Chlorosulfonyl)(methyl)amino]-N,N-dimethylethanaminium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-[(Chlorosulfonyl)(methyl)amino]-N,N-dimethylethanaminium chloride | HCID 86627952 | — |
Reaction Steps
To a solution of sulfuryl chloride (1.0 eq.) in CHCl3 at 0° C. was added dropwise trimethylethylenediamine (1.0 eq.) over 15 mins. After the addition, the cooling bath was removed and the mixture was stirred overnight at RT. The solvent was removed under reduced pressure and the residue was left under high vacuum for 4 h. The crude product was obtained as a pale yellow solid and was used without further purification. 1H NMR (300 MHz, DMSO-d6) δ: 3.46-3.29 (4H, m), 2.83 (6H, s), 2.60 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863294B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-8e19611201884840a2fe3fe5ea13f657 |
| Source note | uspto-grants-2011_01 |