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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722270Generated: October 26, 2026

Triphenylphosphine → HCID 18634268, compound

https://huagongshe.com/reaction/1722270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantPyridinium bromideHCID 11309665—
ReactantHCID 18634269HCID 18634269—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18634268HCID 18634268—

Reaction Steps

1.6 ml of diethyl azodicarboxylate are added dropwise, at 20° C. under argon, to 690 mg of 3-Boc-4(S)-cyclohexylmethyl-2,2-dimethyl-5-(2-hydroxyethyl)oxazolidine, 2.6 g of triphenylphosphine and 1.6 g of pyridinium bromide in 15 ml of CH2Cl2. After 16 h at R.T., H2O is added and the mixture is diluted with 100 ml of CH2Cl2. The organic phase is washed twice with saturated NaHCO3 solution and once with saturated NaCl solution. The organic phase is dried with Na2SO4 and concentrated, and the residue is taken up in a little EA and filtered to remove PPh3. Purification on silica gel provides the title compound (eluent: H/EA 15:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855286
Source datasetuspto-grants-1989_08
ORD IDord-039dd923b5b949f596afb454a72b2464
Source noteuspto-grants-1989_08