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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196692Generated: October 27, 2026

Dichloromethane → 3-Methylthio4-n-propoxy-5-benzyloxybenzaldehyde

https://huagongshe.com/reaction/1196692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-BromopropaneHCID 7840—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methylthio-4-hydroxy-5-benzyloxybenzaldehydeHCID 11778108—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-Methylthio4-n-propoxy-5-benzyloxybenzaldehydeHCID 10471022—

Reaction Conditions

Temperature70 °C

Reaction Steps

64.5 g of 3-methylthio-4-hydroxy-5-benzyloxybenzaldehyde dissolved in a 75 mL of DMF was treated with 50 g of K2CO3 and 32 g of 1-bromopropane and stirred overnight at 70° C. The next day about 1.5 liters of methylene chloride and an equal amount of water was added to the reaction mixture. The organic layer was removed, washed three times with distilled water, dried over MgSO4 and evaporated to yield the title compound as viscous liquid that solidified slowly: NMR (200 MHz, CDCl3) δ 1.02 (t, CH2CH2CH3), 1.82 (m, CH2CH2CH3), 2.48 (s, SCH3), 4.12 (t, OCH2CH3), 5.18 (s, OCH2Ar), 7.26-7.52 (m, ArH), 9.86 (s, ArCHO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114961
Source datasetuspto-grants-1992_05
ORD IDord-f942f9bc83db40faae6215a6b21ca956
Source noteuspto-grants-1992_05