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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298604Generated: October 29, 2026

Phenacyl bromide → HCID 18536787, compound

https://huagongshe.com/reaction/2298604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 18537039HCID 18537039—
SolventAcetoneHCID 180—
ProductHCID 18536787HCID 1853678790%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 150 mg (0.745 mmol) of methyl 4-(aminothioxomethyl)-thiophene-2-carboxylate (as prepared in the previous step) in 6 mL of acetone was added 148 mg (0.745 mmol) of 2-bromoacetophenone. After refluxing for 2 h, the mixture was concentrated by boiling to a volume of ca. 2 mL. The resulting mixture was cooled (−10° C.) and filtered washing with cold acetone (2×0.5 mL). A second crop was obtained from the mother liquors and the combined crops dried to afford the title compound as a beige solid (202 mg, 90%). 1H-NMR (300 MHz, DMSO-d6) δ8.56 (d, 1H, J=1.5 Hz), 8.25 (d, 1H, J=1.5 Hz), 8.18 (s, 1H), 8.04 (d, 2H, J=7 Hz), 7.48 (t, 2H, J=7 Hz), 7.38 (t, 1H, J=7 Hz), and 3.89 (s, 3H). Mass spectrum (MALDI-TOF, α-cyano-4-hydroxycinnamic acid matrix) calcd. for C15H11NO2S2: 302.0 (M+H). Found: 301.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-d083ad0f226546ba9c562ddca43ebe41
Source noteuspto-grants-2002_12