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2,2,2-trifluoro-N-[[2-(hydroxymethyl)phenyl]methyl]acetamide → HCID 178431066、化合物

HRID 1490753
ノート
印刷プレビュー

反応式

HRID 1490753 の反応式
O=C(NCc1ccccc1CO)C(F)(F)F>C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCOC1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.CCCC[N+](CCCC)(CCCC)CCCC.C[OH2+].C[OH2+].Cc1ccc(-c2ccc(CS(=O)(=O)[O-])cn2)nc1.[Ir].[Ir]>CC1(C)OB(c2ccc(CNC(=O)C(F)(F)F)c(CO)c2)OC1(C)C.CC1(C)OB(c2ccc(CO)c(CNC(=O)C(F)(F)F)c2)OC1(C)C
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 1

HCID 251496022,2,2-trifluoro-N-[[2-(hydroxymethyl)phenyl]methyl]acetamide

生成物 2

HCID 178431064HCID 178431064、化合物収率 7%HCID 178431066HCID 178431066、化合物収率 69%

試薬・触媒・溶媒 4

HCID 2733548Bis(pinacolato)diborane試薬HCID 165587889
Tetrabutylazanium {5'-methyl-[2,2'-bipyridin]-5-yl}methanesulfonate
試薬
HCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridium触媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
50 °C

実験手順

Following general procedure F using 2e (58 mg, 0.25 mmol), B2pin2 (127 mg, 0.50 mmol), [Ir(COD)OMe]2 (2.5 mg, 0.00375 mmol) and 1a (3.8 mg, 0.0075 mmol) in THF (1.25 mL). Stirred in vial at 50 °C for 20 hours. Analysis of crude 1 H NMR using internal standard 1,2‐dimethoxyethane showed 10.2:1 meta:para borylation in 80% yield (19% starting material remaining). The crude product was purified by silica gel chromatography (30% EtOAc in Petroleum Ether 40‐60 o C), however this gave a mixture of the borylated products and starting material, which were inseparable on silica (10.5:1:2.0 mixture of meta:para:starting material ratio, as determined by 1 H NMR), as a white solid (76 mg). As the mixture contained 15% of starting material, the isolated yield was corrected by calculating the mass of the starting material in the mixture. Corrected yield for the borylated products was 68 mg, 0.19 mmol, 76%.

出典と根拠

ORDレコード
ord-743eca7abebe49598be8e84cefe080b5
出典データセット
Borylation dataset from Roche
DOI
10.1002/anie.201708967

反応ノート

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