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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5560생성일: 2026년 10월 24일

Bromoacetic Acid → 4-(2-Furyl)-3-oxaoctanoic acid

https://huagongshe.com/ko/reaction/5560

반응식

참여 물질

역할이름HCID투입량
반응물Bromoacetic AcidHCID 6227—
반응물Sodium hydrideHCID 24758—
반응물(S)-1-(2-Furyl)-1-pentanolHCID 54324361—
용매TetrahydrofuranHCID 8028—
생성물4-(2-Furyl)-3-oxaoctanoic acidHCID 19796008—

반응 조건

온도0 °C

반응 단계

NaH (16.3 g, 680.9 mmol) and freshly distilled THF (170 mL) Were stirred at room temperature as (S)-1-(2-furyl)-1-pentanol ([α]25D -17.2°, 30.0 g, 46.0 mmol) in THF (170 mL) was added dropwise. After the addition was complete, the mixture was stirred for 15 m before cautiously heating to reflux for 1 h. The mixture was cooled to 0° C. before adding dropwise a solution of bromoacetic acid (27.3 g, 196.5 mmol) in THF (40 mL). The mixture was refluxed 2 days before cooling and carefully pouring into 600 mL ice water. The aqueous was washed with ether and acidified with HCl to pH 4, and extracted with ether. The combined organic extracts were washed with brine, dried over MgSO4, and evaporated to give a quantitative yield of crude product which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244910
출처 데이터셋uspto-grants-1993_09
ORD IDord-c6c1fca572fe4e32bea0275f2d8b6a26
출처 메모uspto-grants-1993_09