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HRID 1195380생성일: 2026년 10월 25일

Ethyl chloroformate → Ethyl(1-methyl-1h-tetrazol-5-yl)acetate

https://huagongshe.com/reaction/1195380

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물1,5-DimethyltetrazoleHCID 78825—
반응물Acetone cardiceHCID 18522661—
반응물ButyllithiumHCID 178418339—
용매Hydrochloric AcidHCID 313—
용매Sodium ChlorideHCID 5234—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
생성물Ethyl(1-methyl-1h-tetrazol-5-yl)acetateHCID 283414—

반응 단계

To a solution of 1,5-dimethyltetrazole (10 g) in 100 mL of dry tetrahydrofuran and 20 mL of hexamethylphosphoramide at -78° C. (dry ice-acetone) under an argon atmosphere was added dropwise 50 mL (1.2 equivalent) of n-butyllithium (2.5M in hexane). The deprotonation of 1,5-dimethyltetrazole was allowed to proceed at -78° C. for 40 minutes, then at -20° C. for 30 minutes. The anion solution was rechilled to -78° C. and transferred via a cannula over a period of 45 minutes into a cold (-78° C.) solution containing 12 mL of ethyl chloroformate in 50 mL of tetrahydrofuran. The reaction mixture was diluted with aqueous 2N HCl and saturated aqueous solution of sodium chloride and then extracted with ethyl acetate. The residue from the organic extract was purified by silica gel flash chromatography. The appropriate fractions were combined and evaporated to give 4 g of product. The product was further purified by crystallization from ethyl acetate-hexanes to yield 3.52 g (21%) of the title compound; m.p.=64°-66° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05110940
출처 데이터셋uspto-grants-1992_05
ORD IDord-802c977865e64b8eb8b0f8803340a23c
출처 메모uspto-grants-1992_05