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HRID 1394548作成日:2026年10月27日

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

https://huagongshe.com/reaction/1394548

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Benzyl lactateHCID 98054—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物HCID 178516071HCID 178516071—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
生成物Benzyl 2-[(pyridin-2-yl)oxy]propanoateHCID 16098326—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07348456B2
出典データセットuspto-grants-2008_03
ORD IDord-6d0fa835ff6b4a0393ff26662fa4ca7e
出典メモuspto-grants-2008_03