HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896293Generated: October 28, 2026
1,2-Dichloroethane → HCID 22350153, compound
https://huagongshe.com/reaction/896293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydro-4H-pyran-4-one | HCID 121599 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-[1-(Benzenesulfonyl)indol-4-yl]oxyethanamine | HCID 10267837 | — |
| Product | HCID 22350153 | HCID 22350153 | — |
Reaction Steps
A mixture of 2-{[1-(phenylsulfonyl)-1H-indole-4-yl]oxy}ethylamine (0.316 g, 1.0 mmol), tetrahydro-4H-pyran-4-one (0.09 ml, 1.00 mmol) and sodium triacetoxyborohydride (0.312 g, 1.4 mmol) in 1,2-dichloroethane is treated with acetic acid (0.06 ml) at room temperature, stirred under nitrogen for 18 hr, quenched with concentrated aqueous NH4OH and diluted with methylene chloride and water. The aqueous layer is separated and extracted with methylene chloride. The organic layer and extracts are combined, washed with saturated NaCl, dried over Na2SO4, and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/MeOH/NH4OH: 9/1/0.05) to afford the free amine of the title product as a clear oil, 0.36 g (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919354B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-65514b277a5d4d2cbd44014b230553bb |
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| Source note | uspto-grants-2005_07 |
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