HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → tert-butyl N-(2-hydroxy-3-pyrrolidinylpropoxy)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Tert-butyl (oxiran-2-ylmethoxy)carbamate | HCID 18008120 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-butyl N-(2-hydroxy-3-pyrrolidinylpropoxy)carbamate | HCID 56999457 | 88% |
Reaction Steps
A 150 mg (0.79 mmol) portion of tert-butyl N-(2,3-epoxypropoxy)carbamate was dissolved in 1 ml of methanol, and the solution was mixed with 0.08 ml (0.95 mmol) of pyrrolidine and stirred at room temperature for 14 hours. The reaction solution was mixed with a saturated ammonium chloride aqueous solution and extracted with chloroform. The chloroform layer was washed with saturated brine and dried with anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure to obtain 181 mg (yield, 88%) of tert-butyl N-(2-hydroxy-3-pyrrolidinylpropoxy)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316491B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-8ef80e70fc1f4bc3bcd823cf0529077a |
| Source note | uspto-grants-2001_11 |