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HRID 1025321作成日:2026年10月24日

Benzoxazole → tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamate

https://huagongshe.com/ja/reaction/1025321

反応式

関与物質

役割名称HCID仕込み量
反応物BenzoxazoleHCID 9228—
反応物Ammonium ChlorideHCID 25517—
反応物tert-butyl N-((2S)-1-oxobutan-2-yl)carbamateHCID 10241556—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamateHCID 11522383—

反応条件

温度-5 °C

反応手順

Under an atmosphere of argon, benzo[d]oxazole (5 g, 42.0 mmol, Eq: 1.00) was combined with THF (100 ml) to give a light yellow solution. At −5° C. isopropylmagnesium chloride 2M in THF (21.0 ml, 42.0 mmol, Eq: 1.00) was added dropwise. The reaction was stirred for 1.5 h at −5° C. Then (S)-tert-butyl 1-oxobutan-2-ylcarbamate (4.72 g, 25.2 mmol, Eq: 0.6) diluted in 20 ml THF was added. The reaction was stirred overnight at RT. Satd. ammoniumchloride solution (6 ml) was added to the reaction. The THF was evaporated under vacuum. The reaction mixture was poured into 50 ml H2O and extracted with ethyl acetate (2×100 ml). The crude material was purified by flash chromatography (silica gel, 20 g, 0% to 40% ethyl acetate in heptane). The title compound was obtained as a brown gum (5.08 g, 39.5%, MS (m/e)=307.2 [M+H+]).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08729061B2
出典データセットuspto-grants-2014_05
ORD IDord-545695dd0df944b9b559205a855afc46
出典メモuspto-grants-2014_05