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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356830Generated: October 28, 2026

Triethylamine → HCID 59385317, compound

https://huagongshe.com/reaction/2356830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMethyl valinate hydrochlorideHCID 111190—
ReactantHCID 59385296HCID 59385296—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59385317HCID 59385317—

Reaction Conditions

Temperature50 °C

Reaction Steps

3-Methoxy-4′-nitrobiphenyl-4-carboxylic acid (0.28 g, 1.0 mmol) was dissolved in methylene chloride (10 mL), and then oxalyl chloride (0.13 mL, 1.51 mmol) was added, followed by one drop of DMF. The resulting mixture was stirred at 50° C. for 45 min and then concentrated under reduced pressure. The residue was dissolved in methylene chloride (5 mL) and added dropwise to an ice-cold mixture of L-valine methyl ester hydrochloride (0.21 g, 1.2 mmol), methylene chloride (10 mL), and triethylamine (0.57 mL, 4.1 mmol). The resulting solution was stirred at rt for 18 h. The mixture was concentrated under reduced pressure, and the residue was purified by column chromatography (33% EtOAc in hexanes). LC/MS m/z 387.0 (MH+), retention time 3.40 min. 1H NMR (400 MHz, CD2Cl2) δ 1.05 (t, 6H), 2.32-2.39 (m, 1H), 3.78 (s, 3H), 4.10 (s, 3H), 4.71-4.78 (m, 1H), 7.22 (s, 1H), 7.38 (d, 1H), 7.80 (d, 2H), 8.22-8.37 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759376B2
Source datasetuspto-grants-2010_07
ORD IDord-b6167df9c9f647768669f67327d7ff06
Source noteuspto-grants-2010_07