Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424248Generated: November 2, 2026

Isobutyraldehyde → HCID 68156815, compound

https://huagongshe.com/reaction/1424248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyraldehydeHCID 6561—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 4-iodobenzoateHCID 142891—
ProductHCID 68156815HCID 68156815100%

Reaction Steps

To a solution of ethyl 4-iodobenzoate (140 g, 507 mmol) in tetrahydrofuran at −40° C. was added Isopropylmagnesium chloride lithium chloride complex solution (1.0 M in tetrahydrofuran, 429 mL, 558 mmol) dropwise at a rate to maintain the internal temperature below −30° C. The mixture was stirred for 30 minutes at which point isobutyraldehyde (61 g, 710 mmol) was added dropwise while maintaining the temperature below −35° C. The mixture was stirred at this temperature for 15 minutes and then slowly warmed to room temperature. The reaction was quenched with 1N HCl (3 L) and the mixture extracted with ethyl acetate (2 L×2). The combined organics were washed with brine (1 L) and water (1 L), and then dried over anhydrous Na2SO4. This was concentrated in vacuo to give (+/−)-4-(1-hydroxy-3-methyl-butyl)-benzoic acid ethyl ester (120 g, 100%) as an oil. 1H NMR (400 MHz, CDCl3) δ 7.95 (d, J=8.4 Hz, 2H), 7.47 (s, J=7.2 Hz, 2H), 4.76-4.73 (m, 1H), 4.33-4.28 (m, 2H), 1.71-1.60 (m, 2H), 1.46-1.41 (m, 1H), 1.39-1.31 (m, 3H), 0.92-0.87 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927577B2
Source datasetuspto-grants-2015_01
ORD IDord-845e02125d5b4f808175882d7fe6bd68
Source noteuspto-grants-2015_01