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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268890Generated: November 1, 2026

Acetic Acid → HCID 86596992, compound

https://huagongshe.com/reaction/1268890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantMethyl 6-methylnicotinateHCID 231548—
Reactant2-Hydroxy-5-(methylsulfanyl)benzaldehydeHCID 12433397—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 86596992HCID 8659699271.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-hydroxy-5-methylsulfanylbenzaldehyde (5.05 g, 30 mmol) was dissolved in acetic anhydride (8 mL). Methyl 6-methylnicotinate (4.54 g, 30 mmol) and acetic acid (1.7 mL, 30 mmol) were added. The mixture was heated to 120° C. and stirred for 18 hours. The mixture was allowed to cool to room temperature before being poured into water (200 mL). The aqueous mixture was extracted with ethyl acetate (200 mL). The extract was washed with brine, dried over magnesium sulfate and concentrated in vacuo to afford a brown solid. This material was triturated with ethanol to give 6-[E-2-(-2-acetoxy-5-methylsulfanylphenyl)-vinyl]-nicotinic acid, methyl ester as a colourless solid (7.33 g, 71%) δH (300 MHz, DMSO-d6) 9.06 (1 H, d), 8.28 (1 H, dd), 7.77−7.68 (3 H, m), 7.50 (1 H, d), 7.27 (1 H, d), 7.15 (1 H, d), 3.86 (3 H, s), 2.55 (3 H, s), and 2.36 (3 H, s); m/z (ESI+) 344 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199140B2
Source datasetuspto-grants-2007_04
ORD IDord-89e5749702224582a1b436230671a9a6
Source noteuspto-grants-2007_04