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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1005423생성일: 2026년 10월 26일

2-Naphthaleneacetic acid → 2-(2-Naphthyl)acetyl chloride

https://huagongshe.com/reaction/1005423

반응식

참여 물질

역할이름HCID투입량
반응물2-Naphthaleneacetic acidHCID 11393—
반응물Oxalyl chlorideHCID 65578—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-(2-Naphthyl)acetyl chlorideHCID 588115—

반응 단계

To a stirred solution of 2-naphthylacetic acid (0.960 g, 5.15 mmol) in methylene chloride (10 mL) was added oxalyl chloride (0.58 mL, 6.7 mmol) and DMF (1 drop). After 1.5 hours, the solvent was evaporated to give 2-naphthylacetyl chloride. A solution of the 2-naphthylacetyl chloride in THF (3 mL), cooled to -78° C., was slowly cannulated into a stirred solution of the lithium salt of 4 -(S)-(+)-4-isopropyl-2-oxazolidinone (prepared by treating, at -78° C., a solution of 4 -(S)-(+)-4 -isopropyl-2-oxazolidinone (0.60 g, 5.2 mmol) in THF (4 mL) with a solution of butyllithium (1.6 M in hexane) for 15 min). After 2 hours, 10% citric acid and ethyl acetate were added. The organic phase was washed with NaHCO3 and brine, dried (MgSO4), and concentrated. Flash column chromatography of the residue (15% ethyl acetate/hexanes) gave 4 -(S)-4 -isopropyl-3-(2-naphthylacetyl)-2-oxazolidinone as a slightly yellow oil (0.91 g, 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06054470
출처 데이터셋uspto-grants-2000_04
ORD IDord-09a773d7c0d54027b85c272901318732
출처 메모uspto-grants-2000_04