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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825348Generated: October 27, 2026

Ammonium Chloride → (3S,4R)-4-[(1-Ethyl-5-methylpyrazol-3-yl)carbonylmethyl]-3-[(R)-1-tert-butyldimethylsilyloxyethyl]azetidin-2-one

https://huagongshe.com/reaction/1825348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantAzetidonHCID 10935078—
Reactant1-(1-Ethyl-5-methyl-1H-pyrazol-3-yl)ethanoneHCID 22145369—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(3S,4R)-4-[(1-Ethyl-5-methylpyrazol-3-yl)carbonylmethyl]-3-[(R)-1-tert-butyldimethylsilyloxyethyl]azetidin-2-oneHCID 1069115641.9%

Reaction Steps

3-Acetyl-1-ethyl-5-methylpyrazole (3.51 g) in dry tetrahydroturan (THF) (150 ml) under an argon atmosphere was cooled in an acetone/solid carbon dioxide bath and then treated with a 1M solution of lithium bis(trimethylsilyl)amide (50 ml). The mixture was stirred for 45 minutes and then (3R,4R)-4-acetoxy-3-[(1R)-1-tert-butyldimethylsilyloxyethyl]azetidinone (6.6 g) was added as a solid under a blanket of argon. The mixture was stirred in the cold for 3.5 h. Saturated aqueous ammonium chloride was then added, followed by ethyl acetate, and the mixture was allowed to warm to room temperature. A little water was added and the layers were separated and the aqueous layer was re-extracted with ethyl acetate. The combined ethyl acetate extracts were washed with saturated brine, dried and evaporated. Chromatography on silica gel, eluting with ethyl acetate/hexane mixtures gave the title compound (3.65 g), υmax (CH2Cl2) 3411, 1761, 1678, 1376, 1151, and 838 cm−1; δ(CDCl3) 0.064 (6H, s), 0.86 (9H, s), 1.20 (3H,d, J 6.3 Hz), 1.44 (3H, t, J 7.3 Hz), 2.31 (3H, s), 2.89 (1H, dd, J 1.8 & 4.9 Hz), 3.15 (1H, dd, J 10.0 & 17.1 Hz), 3.50 (1H, dd, J3.5 & 17.0 Hz), 4.06-4.25 (4H, m), 6.11 (1H, s), 6.53 (1H, s), (Found m/z 379.2296. C19H33N3O3Si requires m/z 379.2291),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045619B2
Source datasetuspto-grants-2006_05
ORD IDord-c85304adfcbb41c883289d75930e75e9
Source noteuspto-grants-2006_05