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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-chloroethyl) ether | HCID 8115 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6-Aminoindole | HCID 256096 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(1H-Indol-6-yl)morpholine | HCID 21955890 | 82.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685969B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-ffbb58392a274cd18784196b490dea34 |
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| Source note | uspto-grants-2014_04 |
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