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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71222생성일: 2026년 10월 23일

Acetic Acid → 1-(4-Cyanobenzyl)azetidine-3-carboxylic acid

https://huagongshe.com/ko/reaction/71222

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-CyanobenzaldehydeHCID 66042—
반응물3-azetidinecarboxylic AcidHCID 93192—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물1-(4-Cyanobenzyl)azetidine-3-carboxylic acidHCID 5850434975%

반응 단계

A mixture of 4-formylbenzonitrile (2.88 g, 22.0 mmol), azetidine-3-carboxylic acid (2.02 g, 20 mmol), and acetic acid (1.15 mL, 20.0 mmol) in dichloromethane (20 mL) and methanol (80 mL) was stirred at room temperature for 1 h. Sodium triacetoxyborohydride (6.78 g, 32.0 mmol) was added and stirring was continued at room temperature for 18 hr. The volatiles were removed under reduced pressure, and the residue was partitioned between water (50 mL) and diethyl ether (50 mL). The aqueous phase was washed with diethyl ether (50 mL) and was then concentrated to dryness. The residue was dissolved in water (20 mL) and loaded onto a 2.5×20 cm HP-20 column [Preparation of HP-20 Gel: ˜400 ml of dry, unused MCI CHP-20 Gel (75-150 micron) was swelled in methanol for 24 hrs. The gel was filtered and rinsed with 1 liter of methanol. It was then transferred to a bottle for storage under methanol. Immediately before use, the desired amount of gel was rinsed thoroughly with 20 volumes of water]. The column was eluted with 240 mL of water and 400 mL of methanol. The product containing fractions were concentrated and co-evaporated from ethanol and ethyl acetate/heptane to afford 1-(4-cyanobenzyl)azetidine-3-carboxylic acid (3.25 g, 15.0 mmol, 75% yield) as a white solid. MS: (M+H)=217.18. 1H NMR (400 MHz, MeOD) δ ppm 3.39 (m, 1H), 4.08 (m, 4H), 4.32 (s, 2H), 7.63 (d, J=8.3 Hz, 2H), and 7.82 (d, J=8.3 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822510B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-93d2b528ea634561a82c3c704bca3792
출처 메모uspto-grants-2014_09