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HRID 52193생성일: 2026년 10월 24일

Triphenylphosphine → (R)-N,O-bis(phenoxycarbonyl)-N-(3-butyn-2-yl)hydroxylamine

https://huagongshe.com/ko/reaction/52193

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물N,O-Bis-(phenoxycarbonyl)-hydroxylamineHCID 10107329—
반응물HCID 131719946HCID 131719946—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물(R)-N,O-bis(phenoxycarbonyl)-N-(3-butyn-2-yl)hydroxylamineHCID 11099408—

반응 단계

A solution of (2S-trans)-3-methyloxiranemethanol 4-methylbenzenesulfonate (484 mg; 2 mmol), prepared as in step 1, in dry THF (20 ml) was treated at -70° C. to -60° C. with n-BuLi (1.6M in hexane, 7.5 ml, 12 mmol) under an atmosphere of nitrogen. Glacial acetic acid (1 ml) was added after consumption of all the rosylate (monitored by TLC). After 15 min, sodium bicarbonate (600 mg) was added and the reaction mixture was allowed to warm to room temperature. After filtration through Celite, N,O-diphenoxycarbonylhydroxylamine (550 mg, 2.00 mmol) and triphenylphosphine (786 mg, 3.00 mmol) were added to the filtrate. The resulting mixture was treated with DEAD (0.5 ml, 3.0 mmol), taking care that the reaction temperature did not rise above ambient temperature. The reaction mixture was stirred at room temperature for 16 hours and then concentrated in vacuo. The residue was purifed by chromatography on silica-gel (10% ethyl acetate/hexane) to give (R)-N,O-bis(phenoxycarbonyl)-N-(3-butyn-2-yl)hydroxylamine(contaminated with phenol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616596
출처 데이터셋uspto-grants-1997_04
ORD IDord-8acfe5972ea34b25acf7ac20ff24aeb6
출처 메모uspto-grants-1997_04