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HRID 2176270作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-trifluoromethyl-1,2-benziodoxol-3(1H)-oneHCID 24850981—
反応物HCID 86706109HCID 86706109—
触媒168106-25-0HCID 14940315—
溶媒DichloromethaneHCID 6344—
溶媒Chloroform-DHCID 71583—
生成物(R)-2-methyl-2-trifluoromethoxymethyl-but-3-enoic acid methyl esterHCID 8670611423.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09062092B2
出典データセットuspto-grants-2015_06
ORD IDord-6fb46d62428f47cbafe6b18b691cc86d
出典メモuspto-grants-2015_06