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HRID 548662作成日:2026年10月25日

Triphenylphosphine → methyl 3-(benzyloxy)-5-{(1S)-1-methyl-2-[(triisopropylsilyl)oxy]ethoxy}benzoate

https://huagongshe.com/reaction/548662

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物Methyl 3-(benzyloxy)-5-hydroxybenzoateHCID 7472028—
反応物(2R)-1-{[Tri(propan-2-yl)silyl]oxy}propan-2-olHCID 57504697—
溶媒TetrahydrofuranHCID 8028—
生成物methyl 3-(benzyloxy)-5-{(1S)-1-methyl-2-[(triisopropylsilyl)oxy]ethoxy}benzoateHCID 5362962271.4%

反応条件

温度0 °C

反応手順

(2R)-1-[(Triisopropylsilyl)oxy]propan-2-ol (56.1 g, 242 mmol) was added to a solution of methyl 3-hydroxy-5-{[phenylmethyl]oxy}benzoate (50 g, 194 mmol) and triphenylphosphine (63.5 g, 242 mmol) in dry THF (500 mL), at 0° C., followed by addition of DIAD (47.6 mL, 242 mmol) over 45 minutes under an argon atmosphere. The reaction was stirred at 0° C. for 1 hour and allowed to warm up to RT over an hour then stirred at RT for 1 hour. The THF was evaporated and a mixture of ethyl acetate (80 mL) and hexane (120 mL) was added. This mixture stirred for 2 hours and filtered. The precipitate was washed with a mixture of ethyl acetate (20 mL) and hexane (180 mL) and the filtrate evaporated. The residue was purified by column chromatography, eluting with 1:20 to 1:10 ethyl acetate:hexanes, to afford the title compound (65.5 g). 1H NMR δ (CDCl3): 1.05 (s, 18H), 1.05-1.1 (m, 3H), 1.35 (d, 3H), 3.7 (m, 1H), 3.9 (m, 1H), 3.9 (s, 3H), 4.5 (m, 1H), 5.05 (s, 2H), 6.75 (s, 1H), 7.2 (s, 1H). 7.3-7.5 (m, 6H). m/z 471 (M−H)−

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943607B2
出典データセットuspto-grants-2011_05
ORD IDord-f77350a077c24c879c68a2b58d51a996
出典メモuspto-grants-2011_05