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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356676생성일: 2026년 10월 24일

N-Phenylglycine ethyl ester → (4aR-cis)-1,2,3,4a,5,10b-Hexahydro-5,5-dimethyl-3-oxo-1-phenyl[1]benzopyrano[3,4-b][1,4]oxazine-9-carbonitrile

https://huagongshe.com/ko/reaction/356676

반응식

참여 물질

역할이름HCID투입량
반응물N-Phenylglycine ethyl esterHCID 75190—
반응물(3R-trans)-[(6-cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-yl)phenylamino]acetic acid, ethyl esterHCID 10738551—
반응물(1aR,7bR)-2,2-Dimethyl-1a,7b-dihydro-2H-oxireno[2,3-c]chromene-6-carbonitrileHCID 10987295—
반응물TrimethylaluminumHCID 16682925—
용매1,2-DichloroethaneHCID 11—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
용매Ethyl AcetateHCID 8857—
생성물(4aR-cis)-1,2,3,4a,5,10b-Hexahydro-5,5-dimethyl-3-oxo-1-phenyl[1]benzopyrano[3,4-b][1,4]oxazine-9-carbonitrileHCID 67799274—

반응 단계

A solution of N-phenylglycine ethyl ester (900 mg, 5.0 mmol) in 1,2-dichloroethane (10 mL) under argon at 20° C. was treated with trimethylaluminum (3.0 mL, 2.0M in toluene, 6.0 mmol) over 1-2 minutes. After 15 minutes, (1aR-cis)-1a,7b-dihydro-2,2-dimethyl-2H-oxireno[c][1]benzopyran-6-carbonitrile (1.0 g, 5.0 mmol, title A compound of example 3) was added at once and stirring was continued for 1.5 hours. The mixture was diluted with ethyl acetate, quenched with a few drops of water and filtered through celite to remove gelatinous aluminum salts. The filtrate was washed with 5% sodium bicarbonate, water and brine, dried over anhydrous magnesium sulfate and concentrated. The residue was triturated with warm methanol to give warm methanol to give the title product (392 mg), mp 241°-243° C. [α]D =-129.1 ° (c=0.35 CHCl3). Analysis calculated for. C20H18N2O3 ·0.14 H2O: C,71.29; H,5.47; N, 8.31. Found: C, 71.05; H, 5.30; N, 8.55.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05837702
출처 데이터셋uspto-grants-1998_11
ORD IDord-a24d7fadbac848f990d1434e8d45cd9f
출처 메모uspto-grants-1998_11