HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → benzyl 3-aminosulfonyl-2(R)-methylpropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 18738445 | HCID 18738445 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | benzyl 3-aminosulfonyl-2(R)-methylpropionate | HCID 18738444 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A 100 mL round bottom flask equipped with magnetic stir bar was charged with 1.22 g of benzyl 3-chlorosulfonyl-2(R)-methylpropionate in 15 mL CH2Cl2 and cooled to −78° C. To this solution was added to 10 mL of liquid ammonia at −78° C. After 20 minutes the reaction was warmed to room temperature, concentrated in vacuo to afford a white solid. The solid was slurried in ethyl acetate, filtered to remove inorganic salts and concentrated in vacuo to afford 1.08 g of benzyl 3-aminosulfonyl-2(R)-methylpropionate as a clear yellow oil. The crude product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06384036B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-e45199a2a6ee4c15953461ef7c537c80 |
| Source note | uspto-grants-2002_05 |