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N-cyclopropyl-2,2-dimethyl-propanamide → HCID 178447201, 화합물

HRID 1491042
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HRID 1491042 반응식
CC(C)(C)C(=O)NC1CC1>C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCCCC1.CC1(C)OBOC1(C)C.C[OH2+].C[OH2+].Cc1cnc2c(ccc3c(C)c(C)cnc32)c1C.[Ir].[Ir]>CC(C)(C)C(=O)NC1CC1B1OC(C)(C)C(C)(C)O1
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참가 물질

6

반응물 1

HCID 3564968N-cyclopropyl-2,2-dimethyl-propanamide

생성물 1

HCID 178447201HCID 178447201, 화합물수율 67%

시약·촉매·용매 4

HCID 742653,4,7,8-Tetramethyl-1,10-phenanthroline시약HCID 27347684,4,5,5-Tetramethyl[1,3,2]dioxaborolane시약HCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridium촉매
HCID 8078
Cyclohexane
용매

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온도
80 °C

실험 절차

A mixture of 3,4,7,8-tetramethyl-1,10-phenanthroline (46.9 mg, 71 µmol) and [Ir(OMe)(cod)]2 (33.5 mg, 0.14 mmol) in cyclohexane (5 mL) was stirred at room temperature for 15 min in a Schlenk flask under N2 atmosphere. N-Cyclopropylpivalamide (1a: 2.0 g, 14 mmol), 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (HBpin: 3.08 mL, 21 mmol) and cyclohexane (20 mL) were added to the mixture under N2 flow. Then, the reaction mixture was heated at 80 °C for 18 h under N2 atmosphere. The reaction mixture was concentrated in vacuo. The resultant residue was purified by silica gel flash column chromatography (chloroform/acetone = 25:1 to 20:1). The collected fractions were purified again by silica gel column chromatography (hexane/ether = 1:2 to 1:4) to give 2.33 g of the product 2a as a white solid in a 62% yield. NOE was observed between H1 and H2 . This result indicates that boronate 2a has cis configuration.

출처 및 근거

ORD 기록
ord-7c69564111614240be6228854f8b7bd0
출처 데이터셋
Borylation dataset from Roche
DOI
10.1002/anie.201409186

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