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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453438Generated: October 25, 2026

5-Methoxybenzofuran-2-carboxylic acid → 5-methoxy-N-(5-methylhexan-3-yl)benzofuran-2-carboxamide

https://huagongshe.com/reaction/1453438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxybenzofuran-2-carboxylic acidHCID 288638—
Reactant5-Methylhexan-3-amineHCID 22955496—
Product5-methoxy-N-(5-methylhexan-3-yl)benzofuran-2-carboxamideHCID 5752777367%

Reaction Steps

Prepared in a similar manner to example 4 using 5-methoxybenzofuran-2-carboxylic acid and 5-methylhexan-3-amine (example 5a). Yield: 67%. 1H NMR (500 MHz, CDCl3): δ 0.96 (m, 9H); 1.39-1.52 (m, 3H); 1.66 (m, 2H); 3.85 (s, 3H); 4.17 (m, 1H); 6.24 (d, 1H); 7.01 (dd, 1H); 7.08 (d, 1H); 7.38 (m, 2H). MS (290, M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476399B2
Source datasetuspto-grants-2009_01
ORD IDord-abb43cbfdd3d43729e4e729a6500ca50
Source noteuspto-grants-2009_01