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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552296Generated: October 31, 2026

4-Phenyl-5-propyl-thiophene-2-carboxylic acid methoxy-methyl-amide → 1-(4-Phenyl-5-propyl-thiophen-2-yl)-ethanone

https://huagongshe.com/reaction/552296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenyl-5-propyl-thiophene-2-carboxylic acid methoxy-methyl-amideHCID 86640176—
ReactantHCID 178418573HCID 178418573—
SolventWaterHCID 962—
Product1-(4-Phenyl-5-propyl-thiophen-2-yl)-ethanoneHCID 67165130—

Reaction Steps

At 2° C. methylmagnesium bromide (1 mL, 1.7 M in THF) is added to a solution of 4-phenyl-5-propyl-thiophene-2-carboxylic acid methoxy-methyl-amide (900 mg, 3.11 mmol). The mixture stirred for 1 h before another portion (0.2 mL) of the Grignard reagent is added. Stirring is continued for 2 h. The mixture is diluted with water, extracted with EA and the organic extracts are dried over MgSO4 and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 5:4 to give 1-(4-phenyl-5-propyl-thiophen-2-yl)-ethanone (456 mg) as a yellow oil; LC-MS: tR=1.06 min, [M+1]+=245.14, 1H NMR (CDCl3): δ 7.59 (s, 1H), 7.47-7.32 (m, 5H), 2.87-2.81 (m, 2H), 2.54 (s, 3H), 1.76-1.63 (m, 2H), 0.95 (t, J=/.6 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951794B2
Source datasetuspto-grants-2011_05
ORD IDord-7876e186fdaf45a286fdfbc5478001ef
Source noteuspto-grants-2011_05