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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 5-(4-chlorophenyl)-2-methylfuran-3-carboxylic acid | HCID 2742181 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [5-(4-Chlorophenyl)-2-methylfuran-3-yl]methanol | HCID 7245332 | 57.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714008B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-1edd2dd4e82e46f3b9e4c673290a3d50 |
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| Source note | uspto-grants-2010_05 |
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