HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272375Generated: October 31, 2026
4-Methoxybenzenesulfonyl chloride → HCID 10163647, compound
https://huagongshe.com/reaction/272375
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(4-Isopropylphenyl)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-amine | HCID 10519978 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 10163647 | HCID 10163647 | 34% |
Reaction Steps
To a solution of 3-(4-isopropylphenyl)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-amine (0.35 g, 1.08 mmol) and 4-methoxybenzenesulfonyl chloride (0.25 g, 1.19 mmol) in chloroform (5 ml) was added triethylamine (0.16 ml, 1.19 mmol) and the mixture was stirred at room temperature for 14 hours. The solvent was concentrated under reduced pressure. Water (20 ml) was added into the residue and the product was extracted twice with ethyl acetate. The combined organic layers were washed with 1N hydrochloric acid and an aqueous saturated solution of sodium hydrogen carbonate, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to obtain 0.18 g (34% yield) of the title compound. Melting point: 206-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456162B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-47b8d3d30b1f43a98f308de92922ee40 |
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| Source note | uspto-grants-2008_11 |
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