HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 2-(2-nitrobenzenesulfonamido)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | Glycine methyl ester hydrochloride | HCID 122755 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(2-nitrobenzenesulfonamido)acetate | HCID 743502 | — |
Reaction Steps
Glycine methyl ester hydrochloride (15.0 g) was dissolved in dichloromethane, and to the solution triethylamine (26.48 g) was added at 0° C. A solution of 2-nitrobenzenesulfonyl chloride (23.57 g) in dichloromethane (50 mL) was then gradually added dropwise. After the mixture was stirred at room temperature for 2 hours, the reaction mixture was concentrated under reduced pressure, and ethyl acetate was added to the residue. The resultant mixture was washed with 2 M hydrochloric acid, water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resultant crystals were recrystallized from ethyl acetate-hexane to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432957B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-0d55c04c6ee34aff8cfdaeb4d1f92daa |
| Source note | uspto-grants-2002_08 |