돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1452073생성일: 2026년 10월 24일

Carbon Dioxide → Propiolic Acid

https://huagongshe.com/ko/reaction/1452073

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Chloromethyl Methyl EtherHCID 7864—
반응물5-(Bromomethyl)-3-methoxy-1,2-oxazoleHCID 10845405—
반응물3-Diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazoleHCID 22906284—
반응물HCID 178462446HCID 178462446—
용매TetrahydrofuranHCID 8028—
생성물Propiolic AcidHCID 10110—
생성물HCID 178462446HCID 178462446—

반응 단계

Dibromoolefin intermediate XIX is then converted to ethynyl intermediate XX. Treatment of the dibromoolefin intermediate with about two equivalents of n-butyllithium produces the lithium acetylide XX, wherein R13 is Li. This transformation is typically carried out in a polar organic solvent, such as tetrahydrofuran, at a temperature of about -78° C. to about 25° C. The lithium acetylide is reacted with electrophiles, such as methoxymethyl chloride, 5-bromomethyl-3-methoxyisoxazole, 3-diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazole, carbon dioxide, tetrazole disulfide, and the like, to prepare the formula I compounds. In a typical example, the lithium acetylide is treated with solid CO2 at a temperature of about -78° C. to about -60° C. to produce propargylic acid intermediate XX wherein R13 is CO2H. This compound may be further modified as described herein.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05606062
출처 데이터셋uspto-grants-1997_02
ORD IDord-574031d5700748da82256e72eb159a91
출처 메모uspto-grants-1997_02