HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053665Generated: October 30, 2026
HCID 22042580, compound → HCID 22042577, compound
https://huagongshe.com/reaction/2053665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22042580 | HCID 22042580 | — |
| Reactant | HCID 178478191 | HCID 178478191 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22042577 | HCID 22042577 | — |
Reaction Steps
To a solution of 0.2 g of N-methyl-N-(4-trifluoroacetyl-phenyl)-benzenesulfonamide in 10 mL of THF were added 0.7 mL of a 1 M solution 4-chlorophenyl magnesium bromide at −78° C. The resulting mixture was stirred at −78° C. for 4 hr. After this time, the reaction mixture was quenched by the addition of a saturated aqueous solution of ammonium chloride and extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (hexanes:EtOAc, 7:1) to give the title compound. 1H-NMR (CDCl3) δ 2.96 (br s, 1 H), 3.17 (s, 3 H), 7.10-7.59 (m, 13 H). Mass Spectrum (CI+) m/e=456 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07326812B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-5574d0d0b565456cacb7ec6f40b445f6 |
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| Source note | uspto-grants-2008_02 |
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