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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387328Generated: October 31, 2026

2-((R)-3-hydroxy-1,1-dimethyl-3-trifluoromethyl-6-trimethylsilanylhex-5-ynyl)benzamide → 2-((S)-3-hydroxy-1,1-dimethyl-3-trifluoromethylhex-5-ynyl)benzamide

https://huagongshe.com/reaction/2387328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((R)-3-hydroxy-1,1-dimethyl-3-trifluoromethyl-6-trimethylsilanylhex-5-ynyl)benzamideHCID 58026172—
SolventTetrahydrofuranHCID 8028—
Product2-((S)-3-hydroxy-1,1-dimethyl-3-trifluoromethylhex-5-ynyl)benzamideHCID 5802612069.1%

Reaction Steps

To a stirred, ice-cooled, THF solution (100 mL) of 2-((R)-3-hydroxy-1,1-dimethyl-3-trifluoromethyl-6-trimethylsilanylhex-5-ynyl)benzamide (17.8 g, 46.2 mmol) n-tetrabutylammonium fluoride was added (51 mL of 1 M solution in THF, 51 mmol) dropwise via addition funnel. After 30 minutes, the reaction was quenched with 200 mL of 1 M HCl and further diluted with brine. The mixture was extracted with ethyl acetate. The combined extract was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent removed in vacuo. The residue was redissolved in dichloromethane and the solvent evaporated. The residue was then dissolved in 30 mL of diethyl ether and triturated with hexanes. The precipitated solid was filtered. The filtrate was collected and the solvent evaporated, and the residue treated with diethyl ether/hexanes as before to obtain more solid precipitate. The solids were combined and dried in vacuo to give 2-((S)-3-hydroxy-1,1-dimethyl-3-trifluoromethylhex-5-ynyl)benzamide (10 g, 33% over two steps). This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268859B2
Source datasetuspto-grants-2012_09
ORD IDord-45f173db075745ff901c5ff22fc80ca1
Source noteuspto-grants-2012_09