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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891591Generated: October 30, 2026

Acetic Acid → HCID 22242932, compound

https://huagongshe.com/reaction/891591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 22242773HCID 22242773—
ReactantHCID 22243059HCID 22243059—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 22242932HCID 2224293252%

Reaction Steps

To a solution of 3-t-butyldiphenylsilyloxy-1-(4-ethoxycarbonyl-1,3-oxazol-2-yl)azetidine (1.70 g, 3.77 mmol) (obtained as described in Reference Example 21(3)) in benzene (38 ml) was added a solution of 0.67M methylamine-trimethylaluminium in benzene (13.7 ml) at room temperature under an atmosphere of nitrogen, and then the mixture was stirred in water bath (50° C.) for 4 hour. After checking the completion of the reaction, 10% aqueous acetic acid solution (100 ml) was added to the reaction mixture in an ice bath, and the resulting mixture was stirred at room temperature for 30 minutes. The reaction mixture was partitioned between ethyl acetate and water. The obtained organic layer was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using ethyl acetate as the eluant to afford 3-t-butyldiphenylsilyloxy-1-(4-carbamoyl-1,3-oxazol-2-yl)azetidine (0.83 g, yield 52%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-19d4daa0b6c84e5185b7784bd3fa5dea
Source noteuspto-grants-2006_02