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HRID 522515作成日:2026年10月27日

Iodine → 2-(Phenylethynyl)benzo[b]thiophene-3-carbaldehyde

https://huagongshe.com/reaction/522515

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物PhenylacetyleneHCID 10821—
反応物1-Benzothiophene-3-carbaldehydeHCID 227328—
反応物Lithium ChlorideHCID 433294—
反応物2-Iodobenzo[b]thiophene-3-carbaldehydeHCID 86659542—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物2-(Phenylethynyl)benzo[b]thiophene-3-carbaldehydeHCID 5852651963%

反応手順

Benzo[b]thiophene-3-carbaldehyde (27) (162 mg, 1.0 mmol) in THF (2 mL) was added to a solution of TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) at 25° C. and the reaction mixture was then stirred at this temperature for 30 min according to TP 2. I2 (381 mg, 1.5 mmol) dissolved in dry THF (2 mL) was then dropwise added and the resulting mixture was stirred for 0.5 h. To the solution of freshly generated in situ 2-iodobenzo[b]thiophene-3-carbaldehyde, NEt3 (7 mL), Cul (8 mg, 4 mol %), Pd(dba)2 (17 mg, 3 mol %) and P(o-furyl)3 (14 mg, 6 mol %) in THF (2 mL) and phenylacetylene (254 mg, 1.5 mol, 1.5 equiv) were successively slowly added. The reaction mixture was stirred at rt for 2 h. The reaction mixture was quenched with a sat. aq. Na2S2O3 solution (10 mL) and with a sat. aq. NH4Cl solution (20 mL), extracted with diethyl ether (3×50 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/n-pentane, 1:2) furnished compound 29c (165 mg, 63%) as a yellowish solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334237B2
出典データセットuspto-grants-2016_05
ORD IDord-46ec1575041d474d863c095fd3cf2a96
出典メモuspto-grants-2016_05