HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 16069189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 20240767 | HCID 20240767 | — |
| Reactant | HCID 67443705 | HCID 67443705 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 16069189 | HCID 16069189 | 42.3% |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
To the solution of 54 mg (0.28 mmol) (1,3-benzoxazol-2-yloxy)acetic acid in 3 ml chloroform 28 mg (0.28 mmol) 4-methylmorpholine is added. The mixture is cooled to −15° C., 30 mg (0.28 mmol) ethyl chloroformate is dropped to it and the mixture is stirred under cooling for 15 minutes. Then the solution of 83 mg (0.34 mmol) N-(3,4-dichlorobenzyl)-N-(methyl)propane-1,3-diamine in 2 ml chloroform is added and the reaction mixture is stirred for 30 min under cooling and 1 hour at room temperature. The chloroform solution is extracted with 2×10 ml water, the organic phase is dried over sodium sulfate and evaporated in vacuum to obtain 50 mg title compound as an oil. LC/MS[MH+]=422 (C20H21Cl2N3O3 422.31).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044078B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-08629145923d40dea0292ab2336defc8 |
| Source note | uspto-grants-2011_10 |