HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713078Generated: October 29, 2026
Sodium Hydroxide → 4-(Isobutylsulfonyl)benzoic acid
https://huagongshe.com/reaction/713078
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58550723 | HCID 58550723 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(Isobutylsulfonyl)benzoic acid | HCID 24708782 | 105.8% |
Reaction Steps
A mixture of methyl 4-isobutylsulfonylbenzoate (1.0 g, 3.9 mmol), NaOH solution (10 mL of 1 M, 10.00 mmol), and dioxane (10 mL) was heated at 80° C. for 1.5 hours. The reaction mixture was cooled to room temperature, then concentrated in vacuo. The solid residue was dissolved in water and washed with ethyl acetate (1×10 mL). The aqueous layer was acidified with 1N HCl solution and was extracted with ethyl acetate (2×10 mL) and layers were separated. The combined organics were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography using (0-100%) ethyl acetate/hexanes as eluent to give 4-isobutylsulfonylbenzoic acid (1.0 g, 98%). ESI-MS m/z calc. 242.1. found 243.2 (M+1)+; Retention time: 1.73 minutes (3 min run). 1H NMR (400 MHz, CDCl3) δ 8.30 (d, J=8.3 Hz, 2H), 8.05 (d, J=8.3 Hz, 2H), 3.03 (d, J=6.5 Hz, 2H), 2.27 (dt, J=13.3, 6.6 Hz, 1H), 1.08 (d, J=6.7 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181273B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-75015b44f8234ed28595f15d2613daa6 |
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| Source note | uspto-grants-2015_11 |
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