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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739412Generated: November 3, 2026

4-Hydroxybenzaldehyde → HCID 21841070, compound

https://huagongshe.com/reaction/1739412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloropropyl phenyl sulfideHCID 269606—
SolventDimethylformamideHCID 6228—
ProductHCID 21841070HCID 2184107082.3%

Reaction Steps

0.69 g of 4-hydroxybenzaldehyde were dissolved in 30 ml of DMF, and the resultant solution was further added with 0.24 g of 60% NaH while cooling the solution with ice and then stirred for 1 hour after elevating the temperature of the solution to room temperature. Further, the solution was fed dropwise with 1.0 g of 1-chloro-3-phenylthio propane while cooling the solution with ice and then stirred for 1 hour at room temperature and further for a night at 50-60° C. After completed the reaction, the solution reacted was poured into ice-water and extracted with ethyl acetate. The organic layer resulted was then washed with aqueous solution of sodium hydroxide and dried with anhydrous magnesium sulfate, and the solvent used was removed by distillation under reduced pressure, thereby affording 1.2 g of 4-(3-phenylthiopropyloxy)-benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965743
Source datasetuspto-grants-1999_10
ORD IDord-543005b2997143fd94378af7ac570ee1
Source noteuspto-grants-1999_10