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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691339Generated: October 30, 2026

Hydrochloric Acid → 4-(Benzylsulfanyl)benzaldehyde

https://huagongshe.com/reaction/1691339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59255250HCID 59255250—
SolventMethanolHCID 887—
Product4-(Benzylsulfanyl)benzaldehydeHCID 1284246094.6%

Reaction Steps

To a solution of 2-(4-benzylsulfanyl-phenyl)-[1,3]dioxolane (1.06 g, 3.89 mmol) described in Manufacturing Example 205-1-1 in methanol (5 mL) and tetrahydrofuran (5 mL) was added 1 N hydrochloric acid (4.16 mL), which was stirred for 30 minutes at room temperature. The mixture was cooled to 0° C. and neutralized with a saturated sodium hydrogencarbonate aqueous solution, and then extracted with ethyl acetate. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (840 mg). The title compound was used in the following reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-ec6d11a712734b0da7b465b31f4aeb95
Source noteuspto-grants-2012_04