Triethylamine → HCID 66929717, 화합물

온도

-78 °C

Triethylamine (6.85 g, 49.15 mmol) and trimethyl acetyl chloride (6.05 mL, 49.15 mmol) were added dropwise (5 min) to a −78° C. solution of 2-heptenoic acid (6 g, 46.81 mmole) in THF (80 mL). The slurry was stirred at −78° C. for 5 min and then replaced with a 0° C. cooling system. It was stirred at this temperature for 1 h. In a separate flask, a solution of R-(+)-4-benzyl-2-oxazolidinone (8.295 g, 46.81 mmol) was cooled to −78° C. and nBuLi (1.6M, 46.8 mmol) was added dropwise over 10 min. The colorless solution was stirred at this temperature for 45 min and transferred via cannula to a −78° C. solution of the ester. The yellowish slurry was warmed to 25° C. overnight (19 h). An aliquot was taken and TLC (1:1 EtOAc-hexane) indicated that reaction was complete. It was cooled to 0° C. and the reaction was quenched by addition of H2O (20 mL). It was diluted with ethyl acetate (200 mL) and the organic layer was separated. The organic layer was dried over MgSO4, filtered, and concentrated to obtain a crude yellow oil (13.69 g). The crude product was purified by column chromatography, silica gel 230 to 400 mesh, eluent: 1:4 EtOAc-hexane to obtain (4R)-4-benzyl-3-[(E)-2-heptenoyl]-1,3-oxazolidin-2-one as a colorless oil (12.1 g, 92.80%). Mass Spectrum (−ESI): 288 (M−H)−.

1. customreplaced with a 0° C.
2. temperaturecooling system
3. stirringIt was stirred at this temperature for 1 h
4. stirringThe colorless solution was stirred at this temperature for 45 min
5. customtransferred via cannula to a −78° C.
6. temperatureThe yellowish slurry was warmed to 25° C. overnight (19 h)
7. temperatureIt was cooled to 0° C.
8. customthe reaction was quenched by addition of H2O (20 mL)
9. additionIt was diluted with ethyl acetate (200 mL)
10. customthe organic layer was separated
11. dry with materialThe organic layer was dried over MgSO4
12. filtrationfiltered
13. concentrationconcentrated
14. customto obtain a crude yellow oil (13.69 g)
15. customThe crude product was purified by column chromatography, silica gel 230 to 400 mesh, eluent

ORD 기록

ord-bdc7b2eea26f485692f3cb17aec8e0ce

출처 데이터셋

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07691884B2