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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096603Generated: November 2, 2026

3-Methoxypropylamine → HCID 62084770, compound

https://huagongshe.com/reaction/1096603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxypropylamineHCID 1672—
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-2-fluoro-3-nitrobenzeneHCID 75016—
SolventDichloromethaneHCID 6344—
ProductHCID 62084770HCID 6208477078.2%

Reaction Steps

1-Chloro-2-fluoro-3-nitrobenzene (2.85 mmol, 0.500 g) was added to an oven dried 50 mL round-bottomed flask equipped for stifling under nitrogen. Dichlormethane (10 mL) and triethylamine (3.13 mmol, 0.437 mL) were added and the resultant solution was cooled to 0° C. with an ice-bath. 3-Methoxypropan-1-amine (2.85 mmol, 0.292 mL) was then added drop-wise via syringe and the resultant solution was stirred at 0° C. for 1 hr. The ice-bath was removed and the reaction was allowed to warm to room temperature and stirred for 16 hr. The reaction solution was poured into water and extracted twice with dichloromethane (50 mL). The organic layer was collected and water was subsequently removed with anhydrous Na2SO4 and the suspension was filtered. The filtrate was collected, concentrated, and dried in-vacuo affording an orange oil, which was then purified by chromatography on slica gel (10-70% ethyl aetate/hexanes) to afford 2-chloro-N-(3-methoxypropyl)-6-nitroaniline (30A) as a yellow solid (2.23 mmol, 0.542 g, 78% yield). ESI-MS: m/z 245.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138168B1
Source datasetuspto-grants-2012_03
ORD IDord-ce6bf151442c4f2aa9fbbdd27e3ce40a
Source noteuspto-grants-2012_03