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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191513Generated: October 29, 2026

Imidazole → (S)-4-(3-Iodo-2-methylpropyl]-4H-benzo[1,4]oxazin-3-one

https://huagongshe.com/reaction/1191513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-4-(3-Hydroxy-2-methylpropyl]-4H-benzo[1,4]oxazin-3-oneHCID 68915929—
SolventChloroformHCID 6212—
Product(S)-4-(3-Iodo-2-methylpropyl]-4H-benzo[1,4]oxazin-3-oneHCID 6891222480%

Reaction Steps

A reaction flask was charged with (S)-4-(3-Hydroxy-2-methylpropyl]-4H-benzo[1,4]oxazin-3-one (2.52 g, 11.4 mmol), triphenylphosphine (6.12 g, 23.3 mmol), imidazole (1.98 g, 29.1 mmol), and iodine (8.88 g, 35.0 mmol) in CHCl3 (30 mL) and stirred at rt for 20 h. The reaction mixture was washed with saturated sodium thiosulfate, dried over Na2SO4, filtered, and concentrated. The product was purified by flash column chromatography (SiO2; n-heptane/EtOAc 3:1) to give the title compound (3.02 g, 80%). 1H NMR (CDCl3) δ 7.07-7.00 (m, 4H), 4.65-4.55 (m, 2H), 3.94 (dd, J=1.7 Hz, J=6.7 Hz, CH2), 3.23-3.14 (m, 2H), 2.18-2.07 (m, 1H), 1.05 (d, J=6.1 Hz, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680115B2
Source datasetuspto-grants-2014_03
ORD IDord-f979c15a631d4e528d6cc06a3fe2c23c
Source noteuspto-grants-2014_03