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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724023Generated: November 1, 2026

Chlorotriethylsilane → 1-benzyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-1H-indole-2-carbaldehyde

https://huagongshe.com/reaction/1724023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotriethylsilaneHCID 13819—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-benzyl-5-(2,2,2-trifluoro-1-hydroxy-1-trifluoromethyl-ethyl)-1H-indole-2-carbaldehydeHCID 11545818—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1-benzyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-1H-indole-2-carbaldehydeHCID 2108219892%

Reaction Steps

To a solution of 0.33 g (0.82 mmol) of 1-benzyl-5-(2,2,2-trifluoro-1-hydroxy-1-trifluoromethyl-ethyl)-1H-indole-2-carbaldehyde (example 23) in 3 mL of DMF at 0° C. were added 0.15 mL (0.99 mmol) of DBU, followed by 0.17 mL (0.99 mmol) of TESCl. The mixture was stirred at RT overnight and then poured into a mixture of a saturated aqueous solution of NH4Cl and Et2O. The phases were separated and the aqueous one was extracted with Et2O. The combined organic phases were dried over Na2SO4 and evaporated to yield 0.389 g (92%) of 1-benzyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-1H-indole-2-carbaldehyde, MS: 516 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485652B2
Source datasetuspto-grants-2009_02
ORD IDord-7d8b8123ee004f5a8823283c2a2524ff
Source noteuspto-grants-2009_02