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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269343Generated: October 31, 2026

Acetic-formic anhydride → HCID 11245009, compound

https://huagongshe.com/reaction/2269343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic-formic anhydrideHCID 75269—
ReactantHCID 57245995HCID 57245995—
SolventPyridineHCID 1049—
ProductHCID 11245009HCID 1124500981%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (2R,3S)-2-(3-phenyl-1-propyl)-3-(2-tetrahydropyranyloxyamino)butanoic acid (21.4 g, 66.7 mmol) in pyridine (100 mL) at 0° C. is added formic acetic anhydride (30 mL). The resulting solution is allowed to warm to 25° C., stirred for 6 h, and then concentrated to dryness under reduced pressure. The resulting gum is dissolved in EtOAc (300 mL) and washed sequentially with 1 N hydrochloric acid (200 mL) and saturated aqueous sodium chloride solution. The organic layer is dried over anhydrous magnesium sulfate and concentrated under reduced pressure providing (2R,3S)-2-(3-phenyl-1-propyl)-3-(formyl-2-tetrahydropyranyloxyamino)butanoic acid as an oil (18.9 g, 81% yield). ESI-MS m/z 372 (M+Na)+348 (M−1)31 .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329400B1
Source datasetuspto-grants-2001_12
ORD IDord-c4dcdb04caaf45a3a3e81cdb94d2e6f8
Source noteuspto-grants-2001_12