HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583555Generated: October 30, 2026
Tetrahydrofuran → HCID 10427343, compound
https://huagongshe.com/reaction/583555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10242074 | HCID 10242074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10427343 | HCID 10427343 | — |
Reaction Steps
4-(3-Pyridyl)-3,5-difluoroaniline (PREPARATION 2, 625 mg, 3.03 mmol), sodium bicarbonate (382 mg, 4.55 mmol, 1.5 eq) and dry THF (60 ml) are combined. The resulting mixture is placed under an atmosphere of nitrogen and benzylchloroformate (394 μl, 4.55 mmol, 1.5 eq) is added. The reaction is allowed to stir at 20-25°. After this time, the reaction is added to methylene chloride (150 ml) and washed with saturated sodium bicarbonate then brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to a solid which is puried by silica gel chromatography (200 g of silica gel, eluted with acetonitrile/chloroform (3/97-1 l, 5/95-21 l), the title compound is recovered as a solid, mp 188-190°; FTIR (neat) cm-1 3030, 1737, 1642, 1478, 1408, 1231, 1029, 723; MS (EI, m/z) 340, 296, 232, 205, 91, 79; NMR (CD3CL3) δ 8.59, 8.53-8.51, 7.95-7.92, 7.56-7.51, 7.44×7.31, 7.28 and 5.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929248 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-9921b1709aea4476acdd675713c258d5 |
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| Source note | uspto-grants-1999_07 |
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