Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963144Generated: October 30, 2026

Acetonitrile → HCID 66731634, compound

https://huagongshe.com/reaction/1963144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantLithium BromideHCID 82050—
ReactantHCID 66734712HCID 66734712—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 66731634HCID 6673163491%

Reaction Steps

Dimethyl 2-(3-(trifluoromethyl)phenyl)piperidine-1,4-dicarboxylate (1.7 g, 4.92 mmol) was dissolved into acetonitrile (22 mL) and water (0.440 mL), then lithium bromide (3.42 g, 39.38 mmol) was added. Et3N (2.74 mL, 19.69 mmol) was added and the resulting yellow suspension was heated under reflux for 2 h. Water (50 mL) and MTBE (150 mL) were added. The phases were separated and the organic layer was extracted with water (2 times). The pooled water layers were acidified to pH 1 with 3.8 M HCl and extracted with MTBE (2 times). The combined organic layer was dried over Na2SO4, filtered and evaporated yielding 1-(methoxycarbonyl)-2-(3-(trifluoromethyl)phenyl)piperidine-4-carboxylic acid (1.48 g, 91%) as a slightly yellow semi-solid. MS m/z 332 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-4295e9c2de9049dbb0eabaebdea5f594
Source noteuspto-grants-2013_04