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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 894383생성일: 2026년 10월 26일

Phosphate → HCID 70547083, 화합물

https://huagongshe.com/reaction/894383

반응식

참여 물질

역할이름HCID투입량
반응물PhosphateHCID 1061—
반응물4-(2-Tetrahydro-2H-pyranoxy)benzaldehydeHCID 11252736—
반응물2,2-Dimethyl-3alpha-cyano-6alpha-bromopenamHCID 12944713—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
생성물HCID 70547083HCID 70547083—

반응 단계

Activated mossy zinc (500 mg) and zinc dust (100 mg) are added to a solution of 2,2-dimethyl-3α-cyano-6α-bromopenam (522 mg, 2 mmol) and p-(2-tetrahydropyranyloxy)benzaldehyde (750 mg, 3.75 mmol) prepared according to E. Piers, W. deWaal and R. W. Britton, J. Am. Chem. Soc., 93, 5113 (1971) in 1 ml of dry tetrahydrofuran. After stirring vigorously at 50° for 3 hrs., the mixture is allowed to cool and 1 ml of pH 5 phosphate buffer is added. After standing for 10 min., the solids are removed by filtration and washed thoroughly with ethyl acetate. The filtrate is extracted with ethyl acetate. The combined extracts are washed with phosphate buffer and saturated sodium chloride, dried with sodium sulfate and the solvents removed by evaporation. The crude material is purified by chromatography on 60 g of silica gel using 40% acetone/chloroform as eluant to afford 2,2-dimethyl-3α-cyanopenam as a by-product melting at 73°- 75° C. and a mixture of 2,2-dimethyl-3α-cyano-6α-[p-(2-tetrahydropyranyloxy)-α-hydroxybenzyl]penam and 2,2-dimethyl-3α-cyano-6β-[p-(2-tetrahydropyranyloxy)-α-hydroxybenzyl]penam. Separation of the 6α- and 6β-compounds is effected by PLC (10% acetone/toluene; two developments) providing the individual 6α- and 6β-compounds.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04283531
출처 데이터셋uspto-grants-1981_08
ORD IDord-577602433f524b5c8e6340992b1d1d70
출처 메모uspto-grants-1981_08