HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 23370104, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | N-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamide | HCID 23370116 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23370104 | HCID 23370104 | 1,095.8% |
Reaction Steps
N-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamide (0.85 g) and diisopropylamine (0.39 ml) were suspended in dichloromethane (20 ml) and a solution of phenyl chloroformate (16.8 g) in dichloromethane (30 ml) was added dropwise under ice-cooling. After stirring the mixture overnight, the reaction solution was washed with water, saturated saline, dried over anhydrous MgSO4 and the solvent was distilled off. Purification of the residue by a silica gel column chromatography (chloroform:ethyl acetate=10:1) followed by crystallization from hexane/ethyl acetate afforded phenyl N-[2-(3,5-di-t-butyl-4-hydroxybenzoylamino)phenyl]carbamate (12.6 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576335 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-4e8c09844fd24b25af4c01a57dab1cc3 |
| Source note | uspto-grants-1996_11 |