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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluoro-4-nitrobenzyl bromide | HCID 2774661 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 5-tert-Butoxycarbonylamino-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl ester | HCID 66649649 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-tert-Butoxycarbonylamino-3-(3-fluoro-4-nitro-benzyl)-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl ester | HCID 66649634 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093406B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-90f4d31b6ed74d3098faf2a09a833331 |
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| Source note | uspto-grants-2012_01 |
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