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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1388876생성일: 2026년 10월 27일

(4-Carboxybutyl)triphenylphosphonium bromide → (Z)-7,7-dimethyl-8-[(tetrahydro-2H-pyran-2-yl)oxy]-5-octenoic acid

https://huagongshe.com/reaction/1388876

반응식

참여 물질

역할이름HCID투입량
반응물(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
반응물2,2-Dimethyl-3-((tetrahydro-2H-pyran-2-yl)oxy)propanalHCID 13276458—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매HexamethylphosphoramideHCID 12679—
용매Sodium chloride; waterHCID 57417360—
생성물(Z)-7,7-dimethyl-8-[(tetrahydro-2H-pyran-2-yl)oxy]-5-octenoic acidHCID 13276460151.5%

반응 단계

To a suspension of 4.43 g (10 mmols) of (4-carboxybutyl)triphenylphosphonium bromide in 20 ml of hexamethylphosphorictriamide and 28 ml of tetrahydrofuran was added dropwise at 0°-5° C., and under argon, 12 ml of 1.6 M butyllithium in hexane. The reaction mixture turned deep red in color. After stirring for 1 hr. at room temperature, 1.08 g (5.86 mmoles) of 2,2-dimethyl-3-[(tetrahydro-2H-pyran-2-yl)oxy]propanal (H. Marschall, et al., Chem. Ber. 107, 887 (1974)) in 3 ml of tetrahydrofuran was added. The resulting mixture was stirred for 17 hrs. at room temperature and then diluted with brine and extracted with hexane. The aqueous phase was acidified with a saturated solution of oxalic acid and extracted four times with ether. The ether extracts were combined, dried over anhydrous magnesium sulfate, filtered, and the solvent was removed in vacuo to yield 2.4 g of crude (Z)-7,7-dimethyl-8-[(tetrahydro-2H-pyran-2-yl)oxy]-5-octenoic acid which was subsequently converted into the methyl ester derivative by treatment with a freshly prepared ethereal solution of diazomethane. The crude ester (2.35 g), obtained after removal of the solvent, was chromatographed on a silica gel column. A mixture of hexane-ether (7:3) eluted 1.24 g (75.2%) of (Z)-7,7-dimethyl-8-[(tetrahydro-2H-pyran-2-yl)oxy]-5-octenoic acid methyl ester. This material was dissolved in 15 ml of methanol and treated with 0.5 ml of 2 N hydrochloric acid. The mixture was stirred for 3 hrs. at room temperature. Ca. 10 ml of methanol was evaporated in vacuo. The remaining solution was diluted with ether and poured into a saturated solution of sodium bicarbonate. The organic layer was washed with brine, dried (MgSO4), and concentrated under reduced pressure to yield 0.940 g of crude material. Chromatographic purification of the product on a silica gel column yielded 0.610 g (69.8%) of pure (Z)-8-Hydroxy-7,7-dimethyl-5-octenoic acid methyl ester (98.9% pure, by GC).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04434101
출처 데이터셋uspto-grants-1984_02
ORD IDord-15cc35abdaee4f9bb93b75f5eb585d10
출처 메모uspto-grants-1984_02