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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921119생성일: 2026년 10월 25일

Triphenylphosphine → (S)-methyl 5-methyl-2-(pent-4-en-2-yloxy)benzoate

https://huagongshe.com/reaction/921119

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Methyl 5-methylsalicylateHCID 89802—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물(2R)-pent-4-en-2-olHCID 6999724—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(S)-methyl 5-methyl-2-(pent-4-en-2-yloxy)benzoateHCID 11830710190%

반응 단계

To a solution of methyl 2-hydroxy-5-methylbenzoate (1.0 g, 6.02 mmol) in THF (14 ml) were added (R)-(−)-pent-4-en-2-ol (1.037 g, 12.04 mmol) and triphenylphosphine (2.052 g, 7.82 mmol). DIAD (1.521 ml, 7.82 mmol) was added dropwise (exotherm) and the mixture was stirred at rt. After 4.5 h, the mixture was diluted with Et2O and washed with 1N NaOH followed by water (3×'s) then brine, dried (Na2SO4), filtered and concentrated. The yellow oil was purified by flash chromatography (Biotage; 0%-100% EtOAc/hexane; 20 CV) to give (S)-methyl 5-methyl-2-(pent-4-en-2-yloxy)benzoate (1.2664 g, 5.41 mmol, 90% yield) as a yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.58 (d, J=2.2 Hz, 1H), 7.23 (dd, J=8.3, 2.0 Hz, 1H), 6.90 (d, J=8.6 Hz, 1H), 6.03-5.77 (m, 1H), 5.21-4.99 (m, 2H), 4.61-4.35 (m, 1H), 3.89 (s, 3H), 2.60-2.46 (m, 1H), 2.46-2.34 (m, 1H), 2.34-2.25 (m, 3H), 1.34 (d, J=6.1 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273067B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-0623d862063447738561a0cabef1b5ef
출처 메모uspto-grants-2016_03