HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006718Generated: October 31, 2026
HCID 22672861, compound → HCID 22672855, compound
https://huagongshe.com/reaction/1006718
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22672861 | HCID 22672861 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22672855 | HCID 22672855 | — |
Reaction Steps
A mixture of the title F compound, 2-benzyloxy-5-(2,6-dimethyl-4-nitrophenoxy)-N-(2,2-dimethylpropyl)benzenesulfonamide (1.22 g, 2.45 mmol) and palladium on activated carbon (10 wt. %; 250 mg) in 40 mL of THF is stirred under hydrogen atmosphere (H2, 1 atm) for 8 h. The catalyst is removed by vacuum filtration through celite, washed with THF and the combined filtrate and washings are concentrated. The residue is suspended in CH2Cl2 and the product is collected by vacuum filtration, washed with CH2Cl2 and dried to give 5-(4-amino-2,6-dimethyl-phenoxy)-2-hydroxy-N-(2,2-dimethylpropyl)benzenesulfonamide: NMR (DMSO-d6) 0.80 (s, 9H), 1.90 (s, 6H), 2.55 (d, 2H, J=7.5), 4.90 (br s, 2H), 6.31 (s, 2H), 6.87 (br s, 1H), 6.93 (br s, 2H), 6.97 (t, 1H, J=7.5), 10.13 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790978B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-f1f0952c52e34a5990651b3458708fc0 |
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| Source note | uspto-grants-2004_09 |
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