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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491039Generated: October 30, 2026

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

https://huagongshe.com/reaction/1491039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-cyclopropyl-2,2-dimethyl-propanamideHCID 3564968—
Reagent3,4,7,8-Tetramethyl-1,10-phenanthrolineHCID 74265—
ReagentBis(pinacolato)diboraneHCID 2733548—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventCyclohexaneHCID 8078—
ProductHCID 178447201HCID 17844720143%

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.1002/anie.201409186
Source datasetBorylation dataset from Roche
ORD IDord-defae8dd2df74bfcb3476d0e5bc9ca0c
Source noteBorylation dataset from Roche