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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506988Generated: October 31, 2026

Acetic Acid → (1S,2R)-3-(benzyloxy)-1-(2-chlorophenyl)-1-hydroxypropan-2-yl acetate

https://huagongshe.com/reaction/1506988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium cerium-nitrateHCID 57418452—
Reactant(2R,3R)-2-(benzyloxymethyl)-3-(2-chlorophenyl)oxiraneHCID 118140949—
Product(1S,2R)-3-(benzyloxy)-1-(2-chlorophenyl)-1-hydroxypropan-2-yl acetateHCID 11837924034%

Reaction Steps

To a solution of (±)-2-(benzyloxymethyl)-3-(2-chlorophenyl)oxirane (Preparation example 373, 2.9 g, 10.55 mmole) in Acetic acid (55 mL) was added Cerium Ammonium Nitrate (1.15 g, 2.11 mmole) at room temperature. The mixture was stirred for 18 hr at room temperature. The TLC showed complete consumption of SM. The reaction mixture was quenched with sat'NaHCO3 to pH7 at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica ge column to produce the title compound (1.2 g, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221783B2
Source datasetuspto-grants-2015_12
ORD IDord-659fa5bdb0e34050a93ddaef772eba19
Source noteuspto-grants-2015_12