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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820976Generated: November 1, 2026

Tetrahydrofuran → Ethyl 4-(1-hydroxy-2-methylpropyl)benzoate

https://huagongshe.com/reaction/1820976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 4-iodobenzoateHCID 142891—
ReactantHCID 178418918HCID 178418918—
ProductEthyl 4-(1-hydroxy-2-methylpropyl)benzoateHCID 68853898—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of 3.19 g (11.6 mmol) of ethyl 4-iodobenzoate in 10 mL of THF at −40° C. was added 6.4 mL (12.7 mmol) of isopropylmagnesium chloride (2.0 M in THF). After stirring at −40° C. for 1 h, 1.26 mL (13.9 mmol) of isobutylaldehyde was added. After stirring at −40° C. for 1 h, the reaction was quenched by adding 10 mL of saturated NaHCO3. The mixture was warmed to rt and poured into brine (20 mL). The aqueous layer was extracted with CH2Cl2 (3×20 mL). Organic layers were combined, dried over Na2SO4, and concentrated. Chromatography on a Biotage 40M cartridge using 1:9 v/v EtOAc/hexanes as the eluant gave 2.08 g of the title compound: 1H NMR (500 MHz, CDCl3) δ 0.82 (d, J=6.9, 3H), 0.96 (d, J=6.6, 3H), 1.39 (t, J=7.1, 3H), 1.95 (m, 1H), 2.09 (br. s, 1H), 4.36 (q, J=7.1, 2H), 4.45 (d, J=6.4, 1H), 7.37 (d, J=8.2, 2H), 7.99 (d, J=8.3, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605171B2
Source datasetuspto-grants-2009_10
ORD IDord-2530c0533ea64c6ea4cfeb0117b3d03b
Source noteuspto-grants-2009_10