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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2104267생성일: 2026년 10월 26일

Triphenylphosphine → Benzyl 2-[(pyridin-2-yl)oxy]propanoate

https://huagongshe.com/reaction/2104267

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Benzyl lactateHCID 98054—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물HCID 178516071HCID 178516071—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물Benzyl 2-[(pyridin-2-yl)oxy]propanoateHCID 16098326—

반응 단계

To a mixture of 2-hydroxypyridine (2.9 g, 30 mmol), benzyl lactate (5.0 g, 21 mmol) and triphenylphosphine (12 g, 47 mmol) in 100 mL of methylene chloride was added diethylazodicarboxylate (7.8 mL, 45 mmol) at 0° C. The reaction was allowed to warm to room temperature for 4 h. The resulting mixture was diluted with hexane (100 mL) and concentrated with 20 g of silica gel. The material was loaded onto a silica gel column, which was eluted with 10% ethyl acetate in hexane to give the title compound. 1H NMR (500 MHz, CD3OD): δ 8.00 (dd, 1H), 7.68 (ddd, 1H), 7.36-7.28 (m, 5 H), 6.94 (dd, 1H), 6.84 (dd, 1H), 5.30 (q, 1H), 5.18 (s, 2H), 1.59 (d, 3H). LC-MS: m/e 258 (M+H)+ (3.3 min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07576239B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-5aba901a1b9f414e85c914c1df711072
출처 메모uspto-grants-2009_08