Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantMethyl 4-[(4-methylbenzenesulfonyl)oxy]benzoateHCID 1771995—
ReactantHCID 178444609HCID 178444609—
SolventDiethyl EtherHCID 3283—
ProductBenzoic acid, 4-hexyl-, methyl esterHCID 59163383%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026478B2
Source datasetuspto-grants-2006_04
ORD IDord-2ba5223bac5c431aa435d0edd11aabad
Source noteuspto-grants-2006_04