HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795376Generated: October 25, 2026
Tetrahydrofuran → Benzoic acid, 4-hexyl-, methyl ester
https://huagongshe.com/reaction/1795376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Methyl 4-[(4-methylbenzenesulfonyl)oxy]benzoate | HCID 1771995 | — |
| Reactant | HCID 178444609 | HCID 178444609 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzoic acid, 4-hexyl-, methyl ester | HCID 591633 | 83% |
Reaction Steps
A flame-dried two-necked flask is charged under argon with 4-(4-methylbenzenesulfonyloxy)benzoic acid methyl ester (0.50 g, 1.63 mmol), Fe(acac)3 (29 mg, 0.08 mmol), THF (10 mL) and N-methylpyrrolidone (NMP, 0.95 mL). A solution of n-hexylmagnesium bromide (2M in Et2O, 1 mL, 2 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 (298 mg, 83%). The spectroscopic and analytical data are identical to those compiled above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07026478B2 |
|---|
| Source dataset | uspto-grants-2006_04 |
|---|
| ORD ID | ord-2ba5223bac5c431aa435d0edd11aabad |
|---|
| Source note | uspto-grants-2006_04 |
|---|