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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045643Generated: October 29, 2026

2-Bromobenzyl bromide → HCID 59749687, compound

https://huagongshe.com/reaction/1045643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl bromideHCID 76965—
ReactantPotassium ethanethioateHCID 23670855—
SolventAcetoneHCID 180—
ProductHCID 59749687HCID 59749687—

Reaction Steps

To a solution of 2-bromo-benzyl bromide (1 ml, Aldrich 187070) in acetone was added potassium thioacetate (0.9 g, Aldrich 241776) and the mixture refluxed for 2 hr. The reaction mixture was purified on a plug of silica eluting through with further acetone to give thioacetic acid S-(2-bromo-benzyl) ester (1.57 g) 1H-NMR (400 MHz, CDCl3): 2.34 (3H, s), 4.24 (2H, s), 7.09-7.14 (1H, dt), 7.23-7.27 (1H, dt), 7.44-7.46 (1H, dd), 7.54-7.56 (1H, dd).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569301B2
Source datasetuspto-grants-2013_10
ORD IDord-70238789d79b458b97f7ca56c30cf795
Source noteuspto-grants-2013_10