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HRID 1374076생성일: 2026년 10월 25일

Triethylamine → (3-Bromo-2-oxo-piperidin-1-yl)acetic acid benzyl ester

https://huagongshe.com/reaction/1374076

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물O-benzylglycine toluene-p-sulphonateHCID 6451311—
반응물1-Butanaminium, N,N,N-tributyl-, carbonic acid (1:1)HCID 11012140—
반응물2,5-Dibromopentanoyl chlorideHCID 11185032—
용매DichloromethaneHCID 6344—
생성물(3-Bromo-2-oxo-piperidin-1-yl)acetic acid benzyl esterHCID 69484297—

반응 단계

67.7 g (0.2 mol) of glycine benzyl ester tosylate and 61.2 ml (0.44 mol) of triethylamine are dissolved in 200 ml of methylene chloride and added in drops at 0° C. to a solution of 55.7 g (0.2 mol) of 2,5-dibromovaleric acid chloride (Okawara et al. Chem. Pharm. Bull. (1982), (30), 1225) in 200 ml of methylene chloride within 45 minutes, and it is stirred for 18 hours at room temperature. The reaction mixture is now added in drops at 0° C. to a solution of 400 ml of aqueous 32% sodium hydroxide and 2 g of tetrabutylammonium hydrogen carbonate (about 15 minutes), and it is stirred for 30 minutes. Then, the phases are separated, and the aqueous phase is extracted three times with 200 ml of dichloromethane each. The organic phases are dried on sodium sulfate, the solution is evaporated to the dry state and chromatographed on silica gel (methylene chloride). The fractions that contain the product are combined and concentrated by evaporation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07164016B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-9da6f88e5c9d425f975ad89bb11f4551
출처 메모uspto-grants-2007_01