HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795377Generated: October 25, 2026
Tetrahydrofuran → Benzoic acid, 4-hexyl-, methyl ester
https://huagongshe.com/reaction/1795377
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Methyl 4-(((trifluoromethyl)sulfonyl)oxy)benzoate | HCID 5315090 | — |
| Reactant | HCID 178444609 | HCID 178444609 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzoic acid, 4-hexyl-, methyl ester | HCID 591633 | 93% |
Reaction Steps
A flame-dried two-necked flask is charged under argon with 4-(trifluoromethylsulfonyloxy)benzoic acid methyl ester (760 mg, 2.66 mmol), Fe(acac)3 (47 mg, 0.13 mmol), THF (30 mL) and N-methylpyrrolidone (NMP, 1.7 mL). A solution of n-hexylmagnesium bromide (2M in Et2O, 1.7 mL, 3.4 mmol) is added via syringe to the resulting red solution, causing an immediate color change to dark brown and finally to violet. The resulting mixture is stirred for 5 min, the reaction is diluted with Et2O and is carefully quenched upon addition of aq. HCl (1M, ca. 10 mL). Work-up followed by flash chromatography of the crude product as described above provides 4-hexylbenzoic acid methyl ester as a colorless syrup (540 mg, 93%). The spectroscopic and analytical data are identical to those compiled above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026478B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-247077bc74b74d10a2c4b0718a7f4454 |
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| Source note | uspto-grants-2006_04 |
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