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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480292Generated: October 26, 2026

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

https://huagongshe.com/reaction/480292

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, 2.0M 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 numberUS06649657B2
Source datasetuspto-grants-2003_11
ORD IDord-c894fa18238d4e9387df607c0a844d2f
Source noteuspto-grants-2003_11