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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1892046생성일: 2026년 10월 27일

Ethanol → 3-Methyl-3-prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decane

https://huagongshe.com/reaction/1892046

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Propargyl bromideHCID 7842—
반응물Sodium hydrideHCID 24758—
반응물(3-Methyl-1-oxa-4-azaspiro[4.5]decan-3-yl)methanolHCID 278563—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Methyl-3-prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decaneHCID 59565408—

반응 단계

Sodium hydride (55% in dispersion in oil) (0.636 g) was added portion wise to a solution of (3-methyl-1-oxa-4-aza-spiro[4.5]dec-3-yl)-methanol (2.0 g) in dry THF (30 ml) at 0° C. The reaction mixture was stirred at R.T. for 50′. Propargyl bromide (0.972 ml) was added dropwise at 0° C. and the resulting mixture was stirred at R.T. for 2 h 30. Additional sodium hydride (55% in dispersion in oil) (0.047 g) and propargyl bromide (0.081 ml) were added at 0° C. followed by the heating of the reaction mixture at 40-45° C. for 1 hr allowed to reach reaction completion. The reaction mixture was treated with abs. Ethanol (4 ml) and diluted with diethyl ether. The resulting insoluble residue was filtered off and the filtrate was concentrated in vacuo to give 2.89 g of crude residue which was purified by column chromatography (hexane/ethyl acetate 1:1) to yield 2.33 g of 3-Methyl-3prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decane as an orange liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507509B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-0e5c6747128c4bb480cc197d76148dbe
출처 메모uspto-grants-2013_08