HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → Benzyl 2-oxopyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 2-oxopyrrolidine-1-carboxylate | HCID 10932936 | 87% |
Reaction Steps
To a solution of 2-pyrrolidinone (1.7 g, 21 mmol) in dry THF (25 mL), at −78° C., a 2.5 N solution of n-buthyllithium in n-hexane (8.4 mL, 21 mmol) is added. The mixture is stirred for 30′ and then a solution of benzyl chlorformate (3.03 mL, 21 mmol) in dry THF (30 mL) is added dropwise. The reaction mixture is stirred until the reaction is complete, quenched with saturated aqueous NH4Cl and ectracted with diethyl ether (3×). The combined organic phase is washed with brine and dried over anhydrous Na2SO4. Evaporation of the solvent gives 4 g (87%) of a colourless oil that is used without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691818B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-5314c8d9463c4c4a959af046f097c045 |
| Source note | uspto-grants-2010_04 |