HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → HCID 21473106, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 21473103 | HCID 21473103 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21473106 | HCID 21473106 | — |
Reaction Steps
27.3 g of 2-iodo-3-methoxycarbonylbenzenesulfonamide and 9.0 ml of n-butyl isocyanate in 300 ml of absolute acetone are treated with 12 ml of DBU at room temperature and heated at the boil for 3 hours. The reaction solution is cooled to room temperature, concentrated to approximately 1/3 of its volume and poured into 1 l of water. The aqueous phase is acidified with concentrated hydrochloric acid to a pH of 1-2, and the precipitate obtained is filtered off with suction. 31.3 g of methyl 2-iodo-[[[(n-butylamino)carbonyl]amino]sulfonyl]benzoate of melting point 163°-7° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05463081 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-f0186f1970f242b6b671d411a96ad875 |
| Source note | uspto-grants-1995_10 |