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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753921Generated: October 28, 2026

Triethylamine → HCID 66679520, compound

https://huagongshe.com/reaction/1753921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 66679843HCID 66679843—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 66679520HCID 6667952088%

Reaction Steps

8-chloro-9-(2-Fluoroethyl)-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid ethyl ester (15) (5.3 g, 15.0 mmol) was dissolved in methanol (180 mL) and triethylamine (1.8 g, 18.0 mmol, 2.5 mL) and 10% Pd/C (2 g in methanol (20 mL)) were added. The mixture was placed on the Parr hydrogenator and shaken for 18 h under a hydrogen atmosphere. The reaction was filtered through a pad of celite, washed with methanol and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate (300 mL) and washed with 10% aqueous potassium carbonate (200 mL), dried over magnesium sulfate and concentrated in vacuo to give 4.2 g (88%) of 9-(2-Fluoroethyl)-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid ethyl ester (16) as a light brown solid. The structure was confirmed by 13C NMR (75 MHz, CDCl3): δC 14.3, 20.6, 21.8, 27.6, 40.3, 43.3 (d, JCF=23 Hz), 54.9, 60.1, 82.0 (d, JCF=165 Hz), 99.8, 102.1, 107.3, 117.2, 121.8, 134.9, 137.6, 153.8, and 176.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09168317B2
Source datasetuspto-grants-2015_10
ORD IDord-c8856cf8ecf34c9fbf5d500a13f292fb
Source noteuspto-grants-2015_10