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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377485Generated: October 25, 2026

4-Propoxybenzaldehyde → HCID 54039598, compound

https://huagongshe.com/reaction/377485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PropoxybenzaldehydeHCID 79812—
Reactant(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54039598HCID 5403959860%

Reaction Steps

This compound was synthesized from p-propoxybenzaldehyde (3.26 g, 20 mmol, prepared from 1-bromopropane and 4-hydroxybenzaldehyde) and 5-carboxypentyltriphenylphosphonium bromide (9.50 g, 20 mmol) in THF (100 mL) by a Wittig reaction. Crystallization (petroleum ether) afforded the product (3.15 g, 60%) as white crystals (mp: 52-53° C.). IR: 3450-2500, 1730 cm-1 ; 1H-NMR: 1.00 (t, 3H), 1.48 (m, 2H), 1.67 (m, 2H), 1.82 (m, 2H), 2.35 (m, 4H), 3.92 (t, 2H), 5.72+6.05 (m, 1H), 6.35 (d, 1H), 7.05 (q, 4H), 10.40 (bs, 1H). Anal. Calcd. for C16H22O3 : C, 73.25, H, 8.45%. Found: C, 73.15, H, 8.45%. Z:E=30:70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025511
Source datasetuspto-grants-2000_02
ORD IDord-5544e728e3d54ce8ac043b0a7f203479
Source noteuspto-grants-2000_02