HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Butylaniline → Butylphenylcarbamoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Butylaniline | HCID 14310 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Butylphenylcarbamoyl chloride | HCID 11435782 | 191.2% |
Reaction Steps
To a solution of 6.72 g (45 mmol) of butylphenylamine in 50 ml of methylene chloride cooled to 10° C. was added slowly with stirring 6.67 g (22.5 mmol) of triphosgene in 40 ml of methylene chloride. The reaction was allowed to continue at room temperature for 27 hours. The solvent was evaporated and the residue extracted twice with n-hexane. The organic solution was concentrated in vacuo to yield 9.11 g (43.03 mmol) of a yellow oil (96%). 1H-NMR (CDCl3): δ 0.9 (m, 3H), 1.3 (m, 2H), 1.6 (m, 2H), 3.7 (m, 2H), 7.2–7.4 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208501B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-f7940c44d7ad45e3a082c61fa0411355 |
| Source note | uspto-grants-2007_04 |