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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237745생성일: 2026년 10월 25일

Hydrochloric Acid → 4-(1,2,2,6,6-Pentamethyl-1,2,3,6-tetrahydropyridin-4-yl)-phenol

https://huagongshe.com/reaction/237745

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhenolHCID 996—
반응물Ammonium HydroxideHCID 14923—
반응물1,2,2,6,6-Pentamethyl-4-piperidoneHCID 241955—
생성물4-(1,2,2,6,6-Pentamethyl-1,2,3,6-tetrahydropyridin-4-yl)-phenolHCID 6852418334%

반응 조건

온도70 °C

반응 단계

1,2,2,6,6-Pentamethyl-piperidin-4-one (8.64 g, 50.00 mmol) and phenol (4.98 g, 53.00 mmol) were melted together at 60° C. in a 100 mL round bottomed flask after which 13.5 mL of concentrated hydrochloric acid was added dropwise. The yellow solution was stirred at 70° C. for 24 hours. The mixture was poured into a beaker containing ice. Ammonium hydroxide was added carefully while stirring until the pH reached 7˜8. The mixture was extracted with EtOAc five times. The organic phases were combined, dried (Na2SO4) and concentrated. The residue was purified by chromatography on a silica gel column, eluting with 7N NH3 in methanol/dichloromethane to give 4-(1,2,2,6,6-pentamethyl-1,2,3,6-tetrahydropyridin-4-yl)-phenol (4.11 g, 34%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642603B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f69f7ec3095f4145ab52f743f9a5268d
출처 메모uspto-grants-2014_02