Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550157Generated: October 31, 2026

Iodine → HCID 59133070, compound

https://huagongshe.com/reaction/550157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactantethyl N-[2-(trifluoromethoxy)phenyl]carbamateHCID 2781632—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 59133070HCID 5913307073%

Reaction Steps

A 1.4 M solution of sec-butyllithiuni in cyclohexane (3.0 mL) was added drop-wise to a solution of ethyl N-[2-(trifluoromethoxy)phenyl]carbamate (0.5000 g, 0.002006 mol) in THF (9 mL) at −70° C. After stirring for 1 hour a solution of iodine (0.51 g, 0.002 mol) in THF (1.0 mL) was added drop-wise at −70° C. Stirring was continued for another 1 hour then the mixture was quenched with saturated ammonium chloride solution. Water (50 mL) was added and the mixture extracted with diethyl ether (3×40 mL). The combined organic phases was washed with 40% sodium meta-bisulfite solution, water and brine, then dried over Na2SO4 and the solvent removed in vacuo to give the desired product in a 73% yield. 1H NMR (400 MHz, CDCl3): δ 1.29-1.36 (m, 3H), 4.21-4.28 (m, 2H), 6.21 (br, 1H), 7.05 (t, J=8.0 Hz, 1H), 7.30 (m, 1H) and 7.80 (dd, J=6.8, 1.2 Hz, 1H). MS (ES+): m/z 375.78 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943767B2
Source datasetuspto-grants-2011_05
ORD IDord-d336cf42417f4231a032c75638203604
Source noteuspto-grants-2011_05