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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-4-(4-methylthiophen-3-yl)benzoic acidHCID 57993800—
ReactantMethyl 4-[amino(hydroxyimino)methyl]-3-fluorobenzoateHCID 72307476—
ProductHCID 67528391HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-110ebf61def34e53b14c83ddc4ead055
Source noteuspto-grants-2012_06