Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182474Generated: November 3, 2026

1,2-Dichloroethane → HCID 23072474, compound

https://huagongshe.com/reaction/1182474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant8-(2-NAPHTHYL)-8-OXOOCTANOIC ACIDHCID 10945991—
SolventDimethylformamideHCID 6228—
ProductHCID 23072474HCID 2307247456%

Reaction Steps

To a solution of 7-(2-naphthoyl)heptanoic acid 50 g (500 mg, 1.76 mmol) in DMF (10 mL) were added HOBT (309 mg, 2.29 mmol) and EDC (504 mg, 2.64 mmol). The mixture was stirred at room temperature for 1 hour, after which methoxylamine-HCl (176 mg, 2.11 mmol) and triethylamine (300 μL, 2.11 mmol) were added and the solution was stirred at room temperature for 16 hours, then at 45° C. for 2 hours. The DMF was evaporated under high vacuum, deionized water was added, and the mixture was extracted with ethyl acetate (2×30 mL). The combined organic layers were washed with saturated sodium bicarbonate (10 mL), washed with brine (10 mL), and dried (MgSO4). The solvents were removed in vacuo and the title compound 64 (308 mg, 56%) was isolated by recrystallization from acetone. 1H NMR (400 MHz, 5:1 CDCl3:CD3OD): 8.37 (s, 1H), 7.89 (m, 2H), 7.78 (m, 2H), 7.48 (m, 2H), 3.59 (s, 3H), 3.01 (t, J=7.3 Hz, 2H), 1.96 (t, J=7.3 Hz, 2H), 1.67 (m, 2H), 1.54 (m, 2H), 1.31 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288567B2
Source datasetuspto-grants-2007_10
ORD IDord-8270867711d5422b8e77de16d0643d33
Source noteuspto-grants-2007_10