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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906098Generated: October 29, 2026

Tetrahydrofuran → HCID 67404328, compound

https://huagongshe.com/reaction/906098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 53406085HCID 53406085—
SolventMethanolHCID 887—
ProductHCID 67404328HCID 6740432855%

Reaction Steps

4-Amino-2-methyl-3-nitrobenzoic acid (1.87 g, 9.54 mmol) was solubilized in methanol (100 mL) and tetrahydrofuran (100 mL) and was treated with (trimethylsilyl)diazomethane solution (5.3 mL, 10.5 mmol, 2.0M in diethyl ether). After the reaction was shown to be complete, the mixture was concentrated and the residue was purified via column chromatography (silica gel, 5:1 hexanes/ethyl acetate) to give 1.10 g (55% yield) of methyl 4-amino-2-methyl-3-nitrobenzoate. 1H NMR (400 MHz, d6-DMSO): 7.73 (d, 1H), 6.75 (d, 1H), 6.51 (broad s, 2H), 3.75 (s, 3H), 2.37 (s, 3H). MS (EI) for C9H10N2O4: 210 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-d352edf749c441fab6153364f6edaa18
Source noteuspto-grants-2011_09