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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432064Generated: October 30, 2026

3-Chloropropiophenone → HCID 10214453, compound

https://huagongshe.com/reaction/432064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloropropiophenoneHCID 70295—
ReactantHCID 178418750HCID 178418750—
ProductHCID 10214453HCID 1021445382%

Reaction Steps

Diethylzinc addition to 3-chloropropiophenone (0.5 g, 2.97 mmol) was performed according to general procedure B using 10 mol % of Compound B (162.1 mg). The crude product was filtered through a pad of basic alumina with EtOAc (200 mL) to yield 485 mg of 8 (82% yield, 88% ee) as a colorless oil: [α]D 20=−21.0 (c 3.0, MeOH); 1H NMR (CDCl3, 360 MHz) δ 0.76 (dd, J=7.6, 7.6 Hz, 3H), 1.76-1.90 (m, 2H), 2.25-2.34 (m, 2H), 3.20-3.29 (m, 1H), 3.48-3.60 (m, 1H), 7.20-7.39 (m, 5H) ppm; 13C{1H} NMR (CDCl3, 90 MHz) δ 7.55, 36.08, 40.58, 45.46, 77.00, 125.20, 126.92, 128.45, 144.33 ppm; IR (KBr) 3566, 3462, 3087, 3060, 3027, 2969, 2936, 2879, 1602, 1494, 1446, 1340, 1251, 1173, 1124, 1074, 1055, 1031, 1014, 989, 900, 762, 702, 611 cm-1; HRMS calcd for C11H14Cl (—OH)+: 181.0784, found 181.0789 (chlorine splitting pattern observed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660884B2
Source datasetuspto-grants-2003_12
ORD IDord-d427ea30f42649b9ad1cbe478ad83d88
Source noteuspto-grants-2003_12