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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660387Generated: October 27, 2026

2,2-Dimethoxypropane → HCID 68784264, compound

https://huagongshe.com/reaction/660387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DimethoxypropaneHCID 6495—
Reactanttert-butyl (2S,3S,5S)-5-(benzyloxymethyl)-1-(2,2-dimethylhexanamido)-2-hydroxy-6-methylheptan-3-ylcarbamateHCID 59630981—
SolventAcetoneHCID 180—
ProductHCID 68784264HCID 6878426473.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl (2S,3S,5S)-5-(benzyloxymethyl)-1-(2,2-dimethylhexanamido)-2-hydroxy-6-methylheptan-3-ylcarbamate (3.8 g, 7.5 mmol) in acetone (50 mL) was added 2,2-dimethoxy-propane (6.0 g, 57.7 mmol). The resulting mixture was cooled to 0° C., BF3Et2O (100 mg, 0.7 mmol) was added. The reaction mixture was allowed to warm to rt and stirred for 2 h. TLC showed the starting material had been consumed. The reaction mixture was quenched with Et3N. The solvent was removed in vacuo and the residue was partitioned between water and EtOAc. The organic layers were washed with H2O and brine, dried over Na2SO4, and evaporated to produce (4S,5R)-tert-butyl 4-((S)-2-(benzyloxymethyl)-3-methylbutyl)-5-((2,2-dimethylhexanamido)methyl)-2,2-dimethyloxazolidine-3-carboxylate (3.0 g, 73%); MS: 547 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084485B2
Source datasetuspto-grants-2011_12
ORD IDord-c6442da65e1449928fe1856417059ad8
Source noteuspto-grants-2011_12