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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890749Generated: October 28, 2026

Ammonium Chloride → 4-(1-Hydroxy-hexyl)-benzaldehyde

https://huagongshe.com/reaction/890749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Diethoxymethyl)benzaldehydeHCID 595993—
ReactantHCID 178445865HCID 178445865—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Hydroxy-hexyl)-benzaldehydeHCID 22246899369.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-diethoxymethyl-benzaldehyde (0.300 mL, 1.51 mmol) in THF (3 mL) was cooled to 0° C. Pentylmagnesium bromide (3.0 mL, 2.0 M in THF, 6 mmol) was added dropwise. The reaction was stirred at 0° C. for 1 h and was warmed to room temperature. Aqueous NH4Cl (satd) was added and the aqueous solution was extracted with EtOAc. The organic solution was washed with brine, dried (MgSO4), filtered, and concentrated. The residue was dissolved in 10% aqueous acetone (50 mL) and wet Amberlyst-15 resin (1.5 g) was added. The mixture was stirred for 24 h and the resin was filtered off through Celite. The solution was concentrated in vacuo. Purification via flash chromatography (4:1 hexanes:EtOAc) provided the title compound (1.15 g). 1H NMR (400 MHz, CDCl3) δ 9.99 (s, 1H), 7.86 (d, 2H), 7.51 (d, 2H), 4.77 (m, 1H), 1.89 (m, 1H), 1.74 (m, 2H), 1.48–1.28 (m, 6H), 0.87 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998423B2
Source datasetuspto-grants-2006_02
ORD IDord-41cfc791f50644cc9d822550083a082d
Source noteuspto-grants-2006_02