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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1680128생성일: 2026년 10월 26일

4-(Dimethylamino)Benzaldehyde → 2,2-Dimethyl-3alpha-cyano-6alpha-(p-dimethylamino-alpha-hydroxybenzyl)penam

https://huagongshe.com/reaction/1680128

반응식

참여 물질

역할이름HCID투입량
반응물4-(Dimethylamino)BenzaldehydeHCID 7479—
반응물2,2-Dimethyl-3alpha-cyano-6alpha-bromopenamHCID 12944713—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2,2-Dimethyl-3alpha-cyano-6alpha-(p-dimethylamino-alpha-hydroxybenzyl)penamHCID 70545653—
생성물2,2-Dimethyl-3alpha-cyano-6beta-(p-dimethylamino-alpha-hydroxybenzyl)penamHCID 70546902—

반응 단계

A solution of 100 mg 2,2-dimethyl-3α-cyano-6α-bromopenam in 40 ml dry tetrahydrofuran is stirred with 60 mg p-dimethylaminobenzaldehyde and 500 mg zinc for about 12 hours at room temperature. The reaction mixture is then diluted in ethyl acetate, washed with aqueous sodium chloride and dried over anhydrous sodium sulfate. Chromatography of the mixture on silica gel affords, in 11:1 ratio, 2,2-dimethyl-3α-cyano-6α-(p-dimethylamino-α-hydroxybenzyl)penam and 2,2-dimethyl-3α-cyano-6β-(p-dimethylamino-α-hydroxybenzyl)penam. The 6α-compound has the following formula: ##STR39## Utilizing 7α-bromo-4-cyano-3-cephem in the above procedure similarly affords 7α-(p-dimethylamino-α-hydroxybenzyl)-4-cyano-3-cephem.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04272439
출처 데이터셋uspto-grants-1981_06
ORD IDord-c52bc1370f8e42859dc572b0280ac4fa
출처 메모uspto-grants-1981_06