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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20473Generated: October 30, 2026

Acetic Anhydride → HCID 68561129, compound

https://huagongshe.com/reaction/20473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 68562782HCID 68562782—
SolventDichloromethaneHCID 6344—
ProductHCID 68561129HCID 6856112989.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add acetic anhydride (2.13 mmoles; 201.52 μL) to a solution of (2R,5R)-5-[(1S,2S)-2-amino-3-(3-fluoro-5-hydroxy-phenyl)-1-hydroxy-propyl]-2-(2-fluoro-1-fluoromethyl-1-methyl-ethoxy)-morpholine-4-carboxylic acid tert-butyl ester (2.03 mmoles; 1.00 g) and triethylamine (2.23 mmoles; 311.29 μL) in 10 mL dichloromethane at 0° C. (ice bath) and stir the mixture at 0° C. for 1 h. Concentrate under reduced pressure and subject residue to silica gel chromatography eluting with 40:60 to 0:100 hexane/ethyl acetate gradient to give the desired compound as white solid (950.00 mg, 87.53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745438B2
Source datasetuspto-grants-2010_06
ORD IDord-b3a1e75c7a4d4006afddaa4c4daa6522
Source noteuspto-grants-2010_06