Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420264Generated: October 27, 2026

Potassium Carbonate → 5-tert-Butoxycarbonylamino-3-(3-fluoro-4-nitro-benzyl)-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl ester

https://huagongshe.com/reaction/420264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-4-nitrobenzyl bromideHCID 2774661—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant5-tert-Butoxycarbonylamino-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl esterHCID 66649649—
SolventAcetoneHCID 180—
Product5-tert-Butoxycarbonylamino-3-(3-fluoro-4-nitro-benzyl)-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl esterHCID 66649634—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-tert-butoxycarbonylamino-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl ester (2.55 g, 8.08 mmol) in acetone (150 mL) was added K2CO3 (3.38 g, 24.2 mmol) and 4-bromomethyl-2-fluoro-1-nitro-benzene (2.12 g, 8.9 mmol) and the reaction mixture was stirred at 25° C. for 16 h. After dilution with water the product is extracted with EtOAc. Combined extracts were washed with brine, dried over MgSO4 and evaporated. The product obtained as a light yellow solid was suitable for use in the next step: TLC (hexane-EtOAc 1:3) Rf=0.26; HPLC RtA=2.31 min; ESIMS [M+NH4]+=486.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-90f4d31b6ed74d3098faf2a09a833331
Source noteuspto-grants-2012_01