Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350280Generated: October 30, 2026

Iodine → HCID 59909851, compound

https://huagongshe.com/reaction/1350280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 59909746HCID 59909746—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59909851HCID 5990985162.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A suspension of triphenylphosphine (9.49 g, 36.18 mmol), iodine (7.98 g, 31.44 mmol) and triethylamine (8.49 ml, 60.75 mmol) in tetrahydrofuran was cooled to −78° C. then treated with tert-butyl (3R)-6-cyclohexyl-3-({[1-(methoxycarbonyl)-2-oxopropyl]amino}carbonyl)hexanoate (Preparation 172) (4.86 g, 11.80 mmol) over 15 minutes. The mixture was stirred at −78° C. for 30 minutes then at 0–5° C. for 2 hours. The mixture was diluted with water and extracted with dichloromethane. The combined organic layers were dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel eluting with a gradient system of ethyl acetate:pentane (0:100 to 10:90) to afford the title compound as a colourless oil (2.92 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214694B2
Source datasetuspto-grants-2007_05
ORD IDord-e07ab2433a3a4ac69ab9a72d0c38c219
Source noteuspto-grants-2007_05