Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235639Generated: October 29, 2026

Trimethylsilyldiazomethane → [5-(4-Chlorophenyl)-2-methylfuran-3-yl]methanol

https://huagongshe.com/reaction/2235639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant5-(4-chlorophenyl)-2-methylfuran-3-carboxylic acidHCID 2742181—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product[5-(4-Chlorophenyl)-2-methylfuran-3-yl]methanolHCID 724533257.2%

Reaction Steps

To a solution of 5-(4-chlorophenyl)-2-methylfuran-3-carboxylic acid (0.104 g, 0.44 mmol) in THF (2 mL) and MeOH (2 mL) was added TMSCHN2 (2.0 M in Et2O, 0.250 mL). The reaction mixture was stirred for 18 hours at which time it was concentrated in vacuo. The residue was dissolved in 1 ml of THF at 0° C., and a solution of LAH (1.0 M in THF, 0.8 mL) was added. After addition, the reaction was stirred at room temperature for 2 hours, and then water (0.24 mL), 15% aqueous NaOH (0.24 mL), and water (0.72 mL) were added sequentially to the reaction. After 30 minutes, the reaction mixture was filtered through celite, and the filtrate was concentrated to give 53.1 (0.056 g). 1H NMR (400 MHz, CDCl3) δ ppm 7.53-7.63 (m, 2H), 7.31-7.40 (m, 2H), 6.64 (s, 1H), 4.52 (s, 2H), 2.37 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714008B2
Source datasetuspto-grants-2010_05
ORD IDord-1edd2dd4e82e46f3b9e4c673290a3d50
Source noteuspto-grants-2010_05