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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927348Generated: October 30, 2026

Iodine → Benzyl 2-(oxazol-2-yl)propan-2-ylcarbamate

https://huagongshe.com/reaction/927348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 2-methyl-1-oxo-1-(2-oxoethylamino)propan-2-ylcarbamateHCID 86674737—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-(oxazol-2-yl)propan-2-ylcarbamateHCID 7108722730.3%

Reaction Steps

A solution of benzyl 2-methyl-1-oxo-1-(2-oxoethylamino)propan-2-ylcarbamate (2.23 g, 8 mmol) in methylene chloride (50 mL) was added to a freshly prepared solution of PPh3 (3.15 g, 12 mmol), I2 (3.05 g, 12 mmol) and Et3N (2.43 g, 24 mmol) in methylene chloride (100 mL). The resulting mixture was stirred at room temperature until TLC showed the reaction was completed. Then water (150 mL) was added. The organic layer was washed with 5% sodium bisulfite (150 mL×2), brine (150 mL) and dried over anhydrous sodium sulfate. Removal of the solvent under reduced pressure left a yellow oil which was purified by column chromatography (silica gel, 50 g, eluting with 25% ethyl acetate in petroleum ether) to yield the title compound (0.63 g, 30%) as colorless oil; MS: m/e 261.2 [M+H]+. 1H NMR (300 MHz, CDCl3): δ 7.57 (s, 1H), 7.37-7.33 (m, 5H), 7.05 (s, 1H), 5.06 (s, 2H), 1.74 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290451B2
Source datasetuspto-grants-2016_03
ORD IDord-f16cabbc23af48e09f90f86641696e8c
Source noteuspto-grants-2016_03