HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 16112501, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N,N-Diisopropylmethylamine | HCID 547370 | — |
| Reactant | (2R,3R)-2-Methyl-3-phenylaziridine | HCID 11263513 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16112501 | HCID 16112501 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
To (2R,3R)-2-Methyl-3-phenylaziridine (38b, 0.08 g, 0.60 mmol) in CH2Cl2 (3 ml) was is added N,N-Diisopropylmethyamine (0.219 ml, 1.32 mmol) and the reaction mixture was cooled to −10° C. before methansulfonyl chloride (0.051 ml, 0.66 mmol) was added The mixture was stirred for 30 min at −10° C. than at room temperature for 1 h. The crude sample was added to a Chromasil C18 column and was eluted with MeCN/H2O 35-70%, 20 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030340B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-2ce22622c1fd48efba25c20db4b2011a |
| Source note | uspto-grants-2011_10 |