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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822128Generated: November 1, 2026

Benzyl Bromide → HCID 11574384, compound

https://huagongshe.com/reaction/1822128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 46221340HCID 46221340—
SolventDimethylformamideHCID 6228—
ProductHCID 11574384HCID 1157438470.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 0.5 g (1.24 mmol) of ethyl-[4-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-phenyl]-amine in 2 mL of DMF were added 0.3 mL (2.5 mmol) of benzylbromide and the mixture was stirred overnight at 80° C. After distribution between a 2M aqueous solution of NaOH and Et2O, drying of the combined organic phases over Na2SO4 and evaporation, the resulting crude was dissolved in 5 mL of MeOH, treated with 1 mL of a 2M NaOMe-solution in MeOH and stirred for 30 min. Evaporation of the solvent and column chromatography on silica gel with n-heptane/EtOAc 95: 5 gave 0.33 g (70%) of 2-[4-(benzyl-ethyl-amino)-phenyl]-1,1,1,3,3,3-hexafluoro-propan-2-ol, light yellow semisolid, MS: 378 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608721B2
Source datasetuspto-grants-2009_10
ORD IDord-1502f5ca14ba41e4a447d761855f2869
Source noteuspto-grants-2009_10