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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2176270생성일: 2026년 10월 23일

1-trifluoromethyl-1,2-benziodoxol-3(1H)-one → (R)-2-methyl-2-trifluoromethoxymethyl-but-3-enoic acid methyl ester

https://huagongshe.com/ko/reaction/2176270

반응식

참여 물질

역할이름HCID투입량
반응물1-trifluoromethyl-1,2-benziodoxol-3(1H)-oneHCID 24850981—
반응물HCID 86706109HCID 86706109—
촉매168106-25-0HCID 14940315—
용매DichloromethaneHCID 6344—
용매Chloroform-DHCID 71583—
생성물(R)-2-methyl-2-trifluoromethoxymethyl-but-3-enoic acid methyl esterHCID 8670611423.1%

반응 단계

Zinc bis(trifluoromethylsulfonyl)imide (750 mg, 1.2 mmol) and (1-(trifluoromethyl)-1,2-benziodoxol-3(1H)-one (758 mg, 2.4 mmol) were added to a stirred solution of (R)-2-hydroxymethyl-2-methyl-but-3-enoic acid methyl ester (288 mg, 2.0 mmol) in dry deuterochloroform (4 mL) under nitrogen. The reaction mixture was stirred at room temperature under nitrogen in a sealed flask for 5 days. The resulting suspension was diluted with dichloromethane and the supernatant was separated and evaporated. Dichloromethane (5 mL) was added to the residue and the supernatant solution was purified by silica gel chromatography using a gradient of pentane/diethyl ether 10:1 to 5:1 to afford crude (R)-2-methyl-2-trifluoromethoxymethyl-but-3-enoic acid methyl ester (98 mg) as a clear oil which was used in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09062092B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-6fb46d62428f47cbafe6b18b691cc86d
출처 메모uspto-grants-2015_06