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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511620Generated: October 30, 2026

Potassium Sodium Tartrate → 3-{[5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]methyl}cyclobutane-1-carbaldehyde

https://huagongshe.com/reaction/511620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantN-methoxy-N-methyl-3-{[5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]methyl}cyclobutane-1-carboxamideHCID 86666119—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-{[5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]methyl}cyclobutane-1-carbaldehydeHCID 8666611687%

Reaction Steps

DIBAL (0.69 ml, 0.69 mmol, 1M in THF) was added dropwise to a solution of N-methoxy-N-methyl-3-{[5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]methyl}cyclobutane-1-carboxamide in THF at −10° C. whilst stirring. The reaction was continued for 3 hours at −10° C. The reaction mixture was poured onto sat. aq. Rochelle's salt (20 ml), diluted with Et2O (50 ml) and stirred for 30 min. This was then separated and the organic layer was washed with Rochelle's salt (30 ml), sat. NaHCO3, (30 ml) and brine (30 ml). This was dried over Na2SO4, filtered and evaporated to give a colorless gum (190 mg, 87%); MS (ESI+) for C20H27F3N2O2Si m/z 413.6 [M+H]+; HPLC purirty 87% (ret. time, 2.25 min); 1H NMR (500 MHz, CHLOROFORM-d) δH ppm −0.10-0.09 (9H, m), 0.88-1.00 (4H, m), 1.63-1.97 (2H, m), 2.07-2.23 (2H, m), 2.24-2.37 (0H, m), 2.37-2.42 (1H, m), 2.43-2.66 (2H, m), 2.93-3.34 (4H, m), 5.49-5.61 (2H, m), 7.16-7.31 (2H, m), 7.32-7.32 (2H, m), 7.49-7.61 (1H, m), 7.73 (1H, s), 7.83 (1H, d, J=8.35 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096634B2
Source datasetuspto-grants-2015_08
ORD IDord-a8c48dc9205946909a30c0d3ea3d2052
Source noteuspto-grants-2015_08