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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1809생성일: 2026년 10월 23일

Acetic Acid → alpha-(4-Benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol

https://huagongshe.com/ko/reaction/1809

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PivalaldehydeHCID 12417—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-Amino-alpha-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcoholHCID 53931958—
용매EthanolHCID 702—
생성물alpha-(4-Benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcoholHCID 54116645—

반응 단계

A mixture of 2-amino-α-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcohol (9.5 g), pivalaldehyde (3.35 ml), acetic acid (1.85 g) and ethanol (200 ml) was stirred for 30 min. To the mixture was added sodium cyanoborohydride (2.33 g) and the mixture was stirred for 24 h. After the mixture was concentrated in vacuo, the residue was diluted with water (200 ml) and extracted with ethyl acetate (200 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to give α-(4-benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol (10.0 g) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726306
출처 데이터셋uspto-grants-1998_03
ORD IDord-b478747f94e9498ba6d526c52d811437
출처 메모uspto-grants-1998_03