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HRID 894383作成日:2026年10月26日

Phosphate → HCID 70547083、化合物

https://huagongshe.com/reaction/894383

反応式

関与物質

役割名称HCID仕込み量
反応物PhosphateHCID 1061—
反応物4-(2-Tetrahydro-2H-pyranoxy)benzaldehydeHCID 11252736—
反応物2,2-Dimethyl-3alpha-cyano-6alpha-bromopenamHCID 12944713—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 70547083HCID 70547083—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04283531
出典データセットuspto-grants-1981_08
ORD IDord-577602433f524b5c8e6340992b1d1d70
出典メモuspto-grants-1981_08