HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Chlorosulfamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | N-(2-Benzofuranylmethyl)glycine ethyl ester | HCID 13236077 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Chlorosulfamic acid | HCID 24499 | — |
| Product | HCID 59811657 | HCID 59811657 | — |
Reaction Steps
A stock of sulfamyl chloride was prepared by adding formic acid to chlorosulfonyl isocyanate. The sulfamyl chloride was added to a room temperature solution of 104 and triethyl amine in methylene chloride. The reaction was stirred at room temperature overnight. TLC (30% ethyl acetate/hexanes) showed a major spot and a minor product. The reaction was poured into 10% HCl, extracted with methylene chloride, dried over sodium sulfate, filtered, and concentrated to a thick yellow syrup. The crude syrup was adsorbed onto silica and purified by flash chromatography with 15-30% ethyl acetate/hexanes to obtain the final product 105 as a light yellow film.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432292B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-256a13f9157f4a8d8906b05f2808ce09 |
| Source note | uspto-grants-2008_10 |