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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25261생성일: 2026년 10월 23일

3,3-Dimethylbutanal → 2-Benzyloxycarbonylamino-5,5-dimethyl-hex-2-enoic acid methyl ester

https://huagongshe.com/ko/reaction/25261

반응식

참여 물질

역할이름HCID투입량
반응물3,3-DimethylbutanalHCID 76335—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Methyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetateHCID 2734718—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2-Benzyloxycarbonylamino-5,5-dimethyl-hex-2-enoic acid methyl esterHCID 6943370894.4%

반응 단계

N-(Benzyloxycarbonyl)-α-phosphonoglycine trimethyl ester (2 g, 6.0 mmol, 1.0 equiv) was dissolved in dry THF (20 mL). tert-Butylacetaldehyde (0.758 mL, 6.0 mmol, 1.0 equiv) and DBU (0.903 mL, 6.0 mmol, 1.0 equiv) were added and the reaction mixture was stirred for 16 h. The solution was diluted with 100 mL of CH2Cl2 and washed with 1×50 mL water, and 1×50 mL brine. The organic layer was dried over Na2SO4, decanted and concentrated in vacuo to provide 2-benzyloxycarbonylamino-5,5-dimethyl-hex-2-enoic acid methyl ester as a thick oil (1.73 g, 94%) which was used without further purification; MS: 306 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858623B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-b21259ade78c46cb91e2d6a90cf23b15
출처 메모uspto-grants-2005_02