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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63809생성일: 2026년 10월 24일

Acetic Acid → 7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene

https://huagongshe.com/ko/reaction/63809

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물ButanalHCID 261—
반응물Ethyl AcetateHCID 8857—
반응물(+)-gamma-TocopherolHCID 92729—
촉매Sulfuric AcidHCID 1118—
용매WaterHCID 962—
생성물7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthreneHCID 68497100100%

반응 단계

A 25 mL RBF was charged with butyraldehyde (155 mg, 2.16 mmol), AcOH (2 mL) and H2SO4 (1 drop). To the flask was then added a solution of (+)-γ-tocopherol (Ex-1C-1) (300 mg, 0.72 mmol) in AcOH (3 mL) dropwise over 2 h via syringe pump. The reaction was then stirred for 16 h and monitored by TLC (9:1 Hept:EtOAc). The reaction was then diluted with water (15 mL) and extracted with DCM (3×20 mL). The combined organic layers were washed with water (3×15 mL), dried over Na2SO4, filtered and concentrated by rotary evaporation to yield 7,9,10-trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene (Ex-1C-2) as a brownish oil (425 mg, >100%), which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447006B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-128bc00887994050a25505632883fba9
출처 메모uspto-grants-2016_09