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

HRID 1490754
ノート
印刷プレビュー

反応式

HRID 1490754 の反応式
O=C(NCc1ccccc1CO)C(F)(F)F>C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCOC1.CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.C[OH2+].C[OH2+].[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 27%HCID 178431066HCID 178431066、化合物収率 44%

試薬・触媒・溶媒 4

HCID 2733548Bis(pinacolato)diborane試薬HCID 42491874,4'-Di-tert-butyl-2,2'-bipyridyl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 dtbpy (2.0 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 1.4:1 meta:para borylation in 77% 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 (1.6:1:0.52 mixture of meta:para:starting material ratio, as determined by 1 H NMR), as a white solid (73 mg). The yield was corrected to account for the 20% of starting material. Corrected yield for the borylated products was 64 mg, 0.18 mmol, 71%. By subtracting the resonances for the meta isomer, the NMR data of the para isomer can be assigned as follows:

出典と根拠

ORDレコード
ord-f99e01605ed240d6a5daaaa0446264af
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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