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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantMethyl 4-(((trifluoromethyl)sulfonyl)oxy)benzoateHCID 5315090—
ReactantHCID 178444609HCID 178444609—
SolventDiethyl EtherHCID 3283—
ProductBenzoic acid, 4-hexyl-, methyl esterHCID 59163393%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026478B2
Source datasetuspto-grants-2006_04
ORD IDord-247077bc74b74d10a2c4b0718a7f4454
Source noteuspto-grants-2006_04