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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478029Generated: October 30, 2026

Sodium Iodide → 3(S)-benzyloxycarbonylamino-4-cyclohexyl-1-iodobutane-2(R,S)-ol

https://huagongshe.com/reaction/478029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(1(S)-benzyloxycarbonylamino-2-cyclohexyl-ethyl)oxiraneHCID 14158022—
SolventAcetonitrileHCID 6342—
Product3(S)-benzyloxycarbonylamino-4-cyclohexyl-1-iodobutane-2(R,S)-olHCID 14158027—

Reaction Steps

42.3 g of (1(S)-benzyloxycarbonylamino-2-cyclohexyl-ethyl)-oxirane are taken up in 200 ml of acetonitrile and the resulting solution is cooled to 0°. After the addition of 20.9 g of sodium iodide, there are added dropwise at 0°, over a period of 30 minutes, 17.7 ml of trimethylchlorosilane. The mixture is stirred at 0°-3° for 40 minutes and then poured onto 700 ml of ice-cold water. The aqueous mixture is extracted with ether, and the organic phase is washed with 750 ml of 5% aqueous sodium thiosulphate solution and 750 ml of saturated, aqueous sodium chloride solution. After drying over sodium sulphate and concentrating by evaporation, an oily mixture of the title compound is obtained which is further processed directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889869
Source datasetuspto-grants-1989_12
ORD IDord-9cc5f47757d94c74b32a9ab348812d3a
Source noteuspto-grants-1989_12