HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219910Generated: October 27, 2026
3-Methyl-4-(4-methylthiophen-3-yl)benzoic acid → HCID 67528391, compound
https://huagongshe.com/reaction/219910
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methyl-4-(4-methylthiophen-3-yl)benzoic acid | HCID 57993800 | — |
| Reactant | Methyl 4-[amino(hydroxyimino)methyl]-3-fluorobenzoate | HCID 72307476 | — |
| Product | HCID 67528391 | HCID 67528391 | — |
Reaction Steps
The title compound was prepared following procedure described for example 4, step 1, but starting from Intermediate 6 (116.2 mg; 0.50 mmol) and Intermediate 2 (106.1 mg; 0.50 mmol). The reaction mixture was filtered through a SPE NH2 column (2 g) and rinsed with ACN. The filtrate was passed through a SPE SCX column (2 g) and rinsed with ACN. After evaporation of the solvents, the crude product was suspended in ACN, filtrated and washed with cHex dried under vacuo, affording the title compound. 1H NMR (DMSO-d6, 300 MHz) δ 8.35-8.30 (m, 1H), 8.17 (d, J=1.3 Hz, 1H), 8.08-8.01 (m, 2H), 7.95 (dd, J=11.0, 1.3 Hz, 1H), 7.46-7.42 (m, 2H), 7.35 (dd, J=3.2, 1.1 Hz, 1H), 3.93 (s, 3H), 2.24 (s, 3H), 2.01 (s, 3H). LC/MS (Method B): 409.1 (M+H)+. HPLC (Method A) Rt 6.06 min (Purity: 93.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202865B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-110ebf61def34e53b14c83ddc4ead055 |
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| Source note | uspto-grants-2012_06 |
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