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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360157생성일: 2026년 10월 24일

Nitromethane → Ethyl 4,4,4-trifluoro-3-(nitromethyl)butanoate

https://huagongshe.com/ko/reaction/1360157

반응식

참여 물질

역할이름HCID투입량
반응물NitromethaneHCID 6375—
반응물1,1,3,3-TetramethylguanidineHCID 66460—
반응물Ethyl 4,4,4-trifluorobut-2-enoateHCID 141226—
용매Ethyl AcetoacetateHCID 8868—
생성물Ethyl 4,4,4-trifluoro-3-(nitromethyl)butanoateHCID 26836381%

반응 조건

온도0 °C

반응 단계

1.0 g (5.94 mmol) of 4,4,4-trifluoro-2-butenoic acid ethyl ester and 0.15 mL (1.19 mmol) of 1,1,3,3-tetramethyl guanidine and 1.6 mL (29.8 mmol) of nitromethane were mixed. The resulting mixture was cooled to 0° C. and then stirred for 3 hours at room temperature, followed by addition of 100 mL of ethylacetoacetate. The reaction mixture was washed with water, and then an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give 1.1 g (4.80 mmol) of the title compound in a yield of 81%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879848B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-ebabf3d7f64247c4a01f2fcabda03b19
출처 메모uspto-grants-2011_02