HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aziridine → 1-[4-[(Methylsulfonyl)amino]benzoyl]aziridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aziridine | HCID 9033 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-[(Methylsulfonyl)amino]benzoic acid triethylamine salt | HCID 14773550 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-[4-[(Methylsulfonyl)amino]benzoyl]aziridine | HCID 14773549 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
To a solution of 0.343 g (3.16 mmol) of ethyl chloroformate in 0.6 mL of acetone cooled to -10° C. under a nitrogen atmosphere add dropwise a solution of 1.0 g (3.16 mmol) of 4-[(methylsulfonyl)amino]benzoic acid triethylamine salt in 25 mL of acetone. Stir the mixture at -10° C. for 2 h then add slowly a solution of 0.136 g (3.16 mmol) of aziridine in 10 mL of acetone. Stir the reaction mixture for 30 min at ambient temperature after the addition is completed then remove the solvent in vacuo. Flash chromatograph the residue on silica gel with diethyl ether: methylene chloride (2:1), evaporate the solvent from the product containing fractions to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04900841 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-13065a408ff14803a59f1d7169f2735a |
| Source note | uspto-grants-1990_02 |