참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 1,5-Dimethyltetrazole | HCID 78825 | — |
| 반응물 | Acetone cardice | HCID 18522661 | — |
| 반응물 | Dimethyltetrazole | HCID 66618598 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexamethylphosphoramide | HCID 12679 | — |
| 생성물 | Ethyl(1-methyl-1h-tetrazol-5-yl)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05068346 |
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| 출처 데이터셋 | uspto-grants-1991_11 |
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| ORD ID | ord-6a8dc3ec27d94f8c85e04bd87ba2220a |
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| 출처 메모 | uspto-grants-1991_11 |
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