HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11397Generated: October 27, 2026
Iodoethane → N-(Benzensulfonyl)-5-chloro-2-ethylindole
https://huagongshe.com/reaction/11397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 5-Chloro-1-(phenylsulfonyl)indole | HCID 6472650 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(Benzensulfonyl)-5-chloro-2-ethylindole | HCID 21974278 | — |
Reaction Steps
t-BuLi (3.7 mL of 1.7 M solution in pentane) was added dropwise to a solution of N-(benzensulfonyl)-5-chloroindole (1) (J. Org. Chem. 1981, 46, 3859) (1.5 g, 5.14 mmol) in THF (35 mL) at −70° C., under a nitrogen atmosphere. The mixture was stirred for 15 min, allowed to warm to room temperature over 20 min, cooled to −70° C., and treated with a solution of ethyl iodide (0.84 mL, 10.5 mmol) in dry THF (5 mL). The mixture was stirred at −78° C. for 1 h, allowed to warm to room temperature, stirred for 2 h, poured into ice (15 g), and a saturated aqueous NH4Cl solution and then extracted with ether (3×20 mL). The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated in vacuo to give a residue which was purified by flash chromatography (silica gel, cyclohexane/ethyl acetate, 8:2) and crystallization from ethylacetate/cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098233B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-25f95517642f49208b1291046c1ef585 |
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| Source note | uspto-grants-2006_08 |
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