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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603637Generated: November 2, 2026

Prop-2-en-1-yl 4-(bromomethyl)benzoate → HCID 19605229, compound

https://huagongshe.com/reaction/1603637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantProp-2-en-1-yl 4-(bromomethyl)benzoateHCID 19605361—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductHCID 19605229HCID 19605229100%

Reaction Steps

Allyl 4-(bromomethyl)benzoate (98 g, 0.4 moles) in dry dimethylformamide (100 ml) was added dropwise to a cooled suspension of potassium thioacetate (46 g, 0.4 moles) in dry dimethylformamide (200 ml). The cooling bath was removed and the mixture was stirred overnight. The reaction was poured into water and extracted with ethyl acetate (×3). The combined extracts were washed with water and brine. The mixture was dried and evaporated to give allyl 4-(acetylthiomethyl)benzoate as an orange oil (100 g, 100% yield). 1H NMR δ (CDCl3) 2.36 (3H, s, COCH3), 4.13 (2H, s, CH2), 4.82 (2H, m, CH2O), 5.32 (2H, m, CH2CH--), 6.05 (1H, m, CHCH2), 7.35 (2H, d, Ph-H), 7.98 (2H, d, Ph-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990102
Source datasetuspto-grants-1999_11
ORD IDord-d9efaf3a24e0465ebb83fb80bf7230b2
Source noteuspto-grants-1999_11