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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974493생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/974493

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물1,5-DimethyltetrazoleHCID 78825—
반응물Acetone cardiceHCID 18522661—
반응물DimethyltetrazoleHCID 66618598—
반응물ButyllithiumHCID 178418339—
용매Hydrochloric AcidHCID 313—
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 saturate 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 번호US05068346
출처 데이터셋uspto-grants-1991_11
ORD IDord-6a8dc3ec27d94f8c85e04bd87ba2220a
출처 메모uspto-grants-1991_11