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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349986Generated: October 25, 2026

Acetone → Benzyl 2-(benzylsulfanyl)benzoate

https://huagongshe.com/reaction/1349986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant2-Mercaptobenzoic AcidHCID 5443—
ReactantBenzyl BromideHCID 7498—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ProductBenzyl 2-(benzylsulfanyl)benzoateHCID 802018—

Reaction Steps

A solution of thiosalicylic acid 1 (2.0 g, 13.0 mmol) in 13 mL of acetone was treated with 1,8-Diazabicyclo[5.4.0]undec-7-ene (7.8 mL, 52 mmol) and benzylbromide (6.2 mL, 52 mmol). The reaction was stirred at room temperature for 50 minutes. The mixture was concentrated under vacuum to remove the acetone. Water was added and the mixture was extracted with EtOAc (3×). The organic layer was washed with water, brine, dried over MgSO4, filtered and concentrated in vacuo to give a yellow solid without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214678B2
Source datasetuspto-grants-2007_05
ORD IDord-4f96972884874736b17efc4c76b972e0
Source noteuspto-grants-2007_05