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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1026555생성일: 2026년 10월 25일

Dichloromethane → Tert-butyl 3-bromo-2,2-dimethylpropanoic acid

https://huagongshe.com/reaction/1026555

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물tert-ButanolHCID 6386—
반응물DiisopropylcarbodiimideHCID 12734—
반응물3-Bromo-2,2-dimethylpropanoic acidHCID 271932—
촉매Cuprous chlorideHCID 62652—
용매Acetic AcidHCID 176—
생성물Tert-butyl 3-bromo-2,2-dimethylpropanoic acidHCID 86671389—

반응 단계

At room temperature under shielded light, to N,N′-diisopropylcarbodiimide (99.75 g) was added copper(I) chloride (1.57 g), and then tert-butanol (83 ml) was added dropwise over 20 minutes, followed by stirring for 4 days. The supernatant (78 ml) was added dropwise to a dichloromethane suspension (270 ml) of 3-bromo-2,2-dimethylpropanoic acid (49.4 g) at room temperature over 30 minutes, followed by stirring for 18 hours. Acetic acid (18.8 ml) was added, and stirred for 1 hour. The reaction suspension was filtered, and ice water and sodium hydrogen carbonate were added to the filtrate for neutralization. After the precipitate was filtered off, the organic layer separated from the filtrate was washed with saturated sodium hydrogen carbonate, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. After pentane was added to the residue, insolubles were filtered off, and the filtrate was concentrated under reduced pressure to afford tert-butyl 3-bromo-2,2-dimethylpropanoic acid (18.81 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729095B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-f1a6d1ee69184155bc34aff288c88b61
출처 메모uspto-grants-2014_05