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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471870Generated: October 30, 2026

Acetophenone → HCID 67384503, compound

https://huagongshe.com/reaction/1471870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 67384503HCID 6738450358.7%

Reaction Steps

To a solution of acetophenone (5.0 g, 41.6 mmol) in thy toluene (5 mL) was added LiHMDS (42.0 mL, 1.0 M in THF, 42.0 mmol) via syringe at 0° C. under argon. After 5 min, cyclopropanecarbonyl chloride (4.35 g, 41.6 mmol) was added in one portion via syringe. The ice bath was removed and AcOH (2 mL), EtOH (50 mL), and hydrazine hydrate (10 mL, 64% aqueous, 127.8 mmol) was added. The mixture was refluxed for 30 min, cooled to room temperature, and concentrated. The residue was extracted with EtOAc, washed with brine, dried over MgSO4, and purified by silica gel column chromatography to give the title compound as a colorless oil (4.5 g). LCMS m/z=184.7 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 0.71-0.80 (m, 2H), 0.89-1.00 (m, 2H), 1.81-1.98 (m, 1H), 6.22 (s, 1H), 7.11-7.56 (m, 5H), 10.50 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012478B2
Source datasetuspto-grants-2015_04
ORD IDord-8d50e0d1335e46b3b4497d0a3f8257d6
Source noteuspto-grants-2015_04