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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 568903생성일: 2026년 10월 25일

6-Phenylhexanoic Acid → 6-Phenyl-1-hexanol

https://huagongshe.com/reaction/568903

반응식

참여 물질

역할이름HCID투입량
반응물6-Phenylhexanoic AcidHCID 79695—
반응물DiboronHCID 6328200—
용매TetrahydrofuranHCID 8028—
생성물6-Phenyl-1-hexanolHCID 520110—

반응 단계

A solution of 6-phenylhexanoic acid (19.8 mmoles) in sieve dried tetrahydrofuran (5 ml) was reduced with diborane in tetrahydrofuran (30 ml, 29.1 mmoles) at 0° C. for 4 hours to give 6-phenylhexanol. To an ice cold solution of the hexanol (ca. 19.8 mmoles) and carbon tetrabromide (21.98 mmoles) in methylene chloride (50 ml) was added triphenylphosphine (22.30 mmoles) in methylene chloride (50 ml) and the resulting solution was stirred for 2.5 hours. The volatiles were evaporated and the residue was taken up in ether (100 ml), cooled in ice, and filtered The filtrate was evaporated and distilled to afford 6-phenylhexyl bromide as an oil. A mixture of the bromide (8.00 mmoles), salicylaldehyde (8.19 mmoles) and potassium carbonate (9.33 mmoles) in dimethylformamide (10 ml) was heated to 100° C. and maintained at that temperature for one hour. The cooled reaction mixture was taken up in hexane (50 ml) and washed with 5% sodium hydroxide (50 ml) and saturated sodium chloride (50 ml). The organic phase was dried over anhydrous magnesium sulfate and charcoal. Evaporation yielded a colorless oil which was purified by flash chromatography over silica gel with 5% ethyl acetate in hexane as eluant to afford the desired product as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04730005
출처 데이터셋uspto-grants-1988_03
ORD IDord-0c87193f99cd4e06a5b80123a59f7a04
출처 메모uspto-grants-1988_03