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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131359생성일: 2026년 10월 26일

Iodine → Ethyl 2-amino-2-cyanoacetate

https://huagongshe.com/reaction/131359

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물HeptaneHCID 8900—
반응물Ethyl 2-cyano-2-(hydroxyimino)acetateHCID 6399078—
촉매PlatinumHCID 23939—
용매Acetic AcidHCID 176—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-amino-2-cyanoacetateHCID 288716141.1%

반응 단계

Combine ethyl cyanoglyoxylate-2-oxime (20.0 g, 141 mmol) and 5% Pt/C (2.0 g, 10% wt. load) in acetic acid (120 mL) and EtOAc (60 mL) and hydrogenate under 40 psi H2 overnight until the reaction is complete by TLC (5:1/heptane:EtOAc, I2 stain). Carefully filtered the spent catalyst using partial vacuum through glass fiber paper, and rinse with HOAc/EtOAc without allowing the cake to dry out. Concentrate the filtrate in vacuo on a rotovapor to an oil, leaving 25.5 g (96%) of crude amino-cyano-acetic acid ethyl ester as the HOAc salt. Partition a portion (13.0 g) of the HOAc salt between EtOAc (70 mL) and water (35 mL). Stir the biphasic solution and add dropwise aqueous 5N NaOH (16.5 mL) to adjust the pH to 8.0-8.2. Separate the layers, and extract the aqueous layer with more EtOAc (3×25 mL). Combine the organic layer, dry (MgSO4), filter, and concentrate the filtrate to dryness in vacuo on a rotovapor at low bath temperature (30-35° C.) to afford 5.68 g (65%) crude amino-cyano-acetic acid ethyl ester which was used immediately in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384934B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-57b89e166bb64269b2551ecb9cef03d9
출처 메모uspto-grants-2008_06