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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422882Generated: October 29, 2026

Potassium bis(trimethylsilyl)amide → HCID 57701073, compound

https://huagongshe.com/reaction/422882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 66676980HCID 66676980—
SolventTolueneHCID 1140—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 57701073HCID 57701073—

Reaction Conditions

Temperature90 °C

Reaction Steps

KHMDS (0.2 mL, 0.5 M in toluene) was added to a solution of 2-(4-(benzyloxy)phenyl)-2-(2,6-difluorophenyl)cycloheptanone (50 mg) in toluene (3 mL) and DMPU (1 mL). The reaction mixture was heated at 90° C. for 2 h (TLC indicated some conversion of the starting material). Additional heating for 1 h gave no further conversion of the starting material according to TLC. The organic phase was washed with water (10 mL), brine, dried (Na2SO4) and concentrated in vacuo. Work-up by flash chromatography (eluent heptane dichloromethane 1:1) afforded the title compound 22 in a yield of 20 mg. 1H-NMR (400 MHz, CDCl3): δ ppm 7.49-7.46 (m, 2H), 7.50-7.34 (m, 5H), 7.10-7.00 (m, 1H), 6.96-6.91 (m, 2H), 6.61-6.59 (m, 1H), 6.53-6.48 (m, 1H), 5.73 (dd, J=5, 9 Hz, 1H), 5.02 (s, 2H), 3.07-3.02 (m, 1H), 2.00-1.20 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101651B2
Source datasetuspto-grants-2012_01
ORD IDord-b8c75e83633d444a96e11b8dc4c5943c
Source noteuspto-grants-2012_01