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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361236Generated: October 31, 2026

Bis(2-chloroethyl) ether → 4-(1H-Indol-6-yl)morpholine

https://huagongshe.com/reaction/2361236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-chloroethyl) etherHCID 8115—
ReactantSodium CarbonateHCID 10340—
Reactant6-AminoindoleHCID 256096—
ReactantEthyl acetate hexaneHCID 21226206—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product4-(1H-Indol-6-yl)morpholineHCID 2195589082.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1H-indol-6-amine (3.14 g, 23.76 mmol), 1-chloro-2-(2-chloroethoxy)ethane (4.18 mL, 35.6 mmol), and sodium carbonate (10.07 g, 95 mmol) in t-BuOH (90 mL) was heated at 100° C. in a pressure tube for 3.5 days. On cooling to room temperature, the mixture was diluted with ethyl acetate and filtered through CELITE®. The filtrate was concentrated under vacuum to dryness. To the residue was added water (50 mL). The mixture was adjusted to pH 11 with saturated NaHCO3 solution and extracted with CH2Cl2 (4×80 mL). The combined extract was washed with brine (50 mL) and dried over anhydrous MgSO4. The desired product (3.96 g, 19.58 mmol, 82% yield) was isolated as a beige solid with ISCO (300 g silica gel, solid loading, 20-50% ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685969B2
Source datasetuspto-grants-2014_04
ORD IDord-ffbb58392a274cd18784196b490dea34
Source noteuspto-grants-2014_04