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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276693생성일: 2026년 10월 26일

Ethanolamine → (4S)-4-Isobutyl-2-isopropyloxazolidine

https://huagongshe.com/reaction/276693

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물IsobutyraldehydeHCID 6561—
반응물(+)-L-Leucine methyl esterHCID 65105—
반응물L-LeucinolHCID 111307—
생성물(4S)-4-Isobutyl-2-isopropyloxazolidineHCID 45096513—

반응 단계

(L)-Leucine methyl ester was reduced to (1S)-1-(hydroxymethyl)-3-methylbutylamine according to Method B1b, Step 2. The 2-hydroxyethylamine was reacted with isobutyraldehyde according to Method B4c, Step 1 to afford (4S)-2-isopropyl-4-isobutyl-1,3-oxazolidine. The oxazolidine was reduced according to Method B4c, Step 2 to give (1S)-1-(hydroxymethyl)-N-isobutyl-3-methylbutylamine. 4-Amino-3-ethylbenzonitrile was converted to 4-cyano-2-ethylformanilide according to Method A3a, Step 1. The formanilide was reacted with SOCl2 and SO2Cl2 according to Method A3a, Step 2 to give 4-cyano-2-ethylphenyl isocyanide dichloride. The substituted 2-hydroxyethylamine was reacted with 4-cyano-2-ethylphenyl isocyanide dichloride according to Method C7b to afford (4S)-2-(4-cyano-2-ethylphenylimino)-3,4-diisobutyl-1,3-oxazolidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06353006B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-c0e79a3d5de447a2ac3ee62c6d7421a8
출처 메모uspto-grants-2002_03