戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1795376作成日:2026年10月27日

Tetrahydrofuran → Benzoic acid, 4-hexyl-, methyl ester

https://huagongshe.com/reaction/1795376

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物Methyl 4-[(4-methylbenzenesulfonyl)oxy]benzoateHCID 1771995—
反応物HCID 178444609HCID 178444609—
溶媒Diethyl EtherHCID 3283—
生成物Benzoic acid, 4-hexyl-, methyl esterHCID 59163383%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07026478B2
出典データセットuspto-grants-2006_04
ORD IDord-2ba5223bac5c431aa435d0edd11aabad
出典メモuspto-grants-2006_04