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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167268Generated: October 27, 2026

m-Chloroperbenzoic acid → HCID 59815816, compound

https://huagongshe.com/reaction/1167268

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBis(benzyloxy)(diisopropylamino)phosphineHCID 196621—
Reactant[(3aS,4R,6aR)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-4-yl] N-[(1S,2R)-3-[1,3-benzodioxol-5-ylsulfonyl-(4-cyano-2,2-dimethyl-butyl)amino]-1-benzyl-2-hydroxy-propyl]carbamateHCID 480324—
ReactantHCID 178418441HCID 178418441—
SolventDichloromethaneHCID 6344—
ProductHCID 59815816HCID 59815816—

Reaction Steps

A solution of {(1S,2R)-3-[(Benzo[1,3]dioxole-5-sulfonyl)-(4-cyano-2,2-dimethyl-butyl)-amino]-1-benzyl-2-hydroxy-propyl}-carbamic acid (3R,3aS,6aR)hexahydro-furo[2,3-b]furan-3-yl ester (0.077 g, 0.12 mmol) and 1H-tetrazole (0.012 g, 0.17 mmol) in CH2Cl2 was treated with dibenzyl diisopropylphosphoramidite (0.050 ml, 0.015 mmol) and stirred at ambient temperature under argon. After 2 h 3-chloroperoxybenzoic acid (0.072 g, 0.30 mmol) was added and the reaction mixture stirred an additional 1 h. Solvent was removed in vacuo, the residue taken up in EtOAc, washed with sat. aq. NaHCO3, and brine. The organic phase was dried over MgSO4, filtered and solvent removed in vacuo to give desired product, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617350B2
Source datasetuspto-grants-2003_09
ORD IDord-e14a31ef159243ff9c1a72201d1a75de
Source noteuspto-grants-2003_09