HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Diethylaniline → HCID 13150467, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3,5-Bis[(propan-2-yl)oxy]aniline | HCID 13457859 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13150467 | HCID 13150467 | 70.7% |
Reaction Steps
3,5-Diisopropyloxyaniline (2 g) and diethylaniline (1.5 g) were dissolved in benzene (20 ml). To the resultant mixture was dropwise added ethyl chloroformate (1.2 g) under ice-cooling. After being allowed to stand at room temperature for 12 hours, the reaction mixture was poured into ice water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel chromatography using a mixture of benzene and tetrahydrofuran as the eluent to give ethyl N-(3,5-diisopropyloxyphenyl)carbamate (1.9 g) in a yield of 67.6%. M.P., 81.5°-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04501756 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-189654e5bbb54e148746d2f79d42d8a7 |
| Source note | uspto-grants-1985_02 |