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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378581Generated: November 1, 2026

Dichloromethane → 4-(4-Bromophenyl)butanethioamide

https://huagongshe.com/reaction/1378581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHexaneHCID 8058—
ReactantLawesson's reagentHCID 87949—
Reactant4-(4-Bromophenyl)butanamideHCID 4417735—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product4-(4-Bromophenyl)butanethioamideHCID 5413213322.2%

Reaction Steps

To a solution of 4-(4-bromophenyl)butyramide (1.653 g, 6.827 mmol) in toluene (35 mL) was added Lawesson's reagent (1.381 g, 3.414 mmol). The reaction was refluxed overnight, cooled to room temperature, and concentrated yielding an orange oil. Flash chromatography of this oil (1:1 hexane:methylene chloride with 1% acetic acid) yielded 4-(4-bromophenyl) thiobutyramide as off-white needles (0.196 g): mp 104°-105° C. 1H NMR (DMSO-d6) 300 mHz δ9.33 (br s, 1H), 9.12 (br s, 1H), 7.44 (d, J=8.11 Hz, 2H), 7.14 (d, J=8.48 H z, 2H), 2.56-2.41 (m, 4H), 1.95-1.85 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668161
Source datasetuspto-grants-1997_09
ORD IDord-777398cd28d34a6ea7704877434bc80f
Source noteuspto-grants-1997_09