HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909427Generated: October 26, 2026
Methyl fluoroacetate → HCID 178520914, compound
https://huagongshe.com/reaction/1909427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl fluoroacetate | HCID 9959 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 178479251 | HCID 178479251 | — |
| Reactant | HCID 178504318 | HCID 178504318 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178520914 | HCID 178520914 | 66.7% |
Reaction Steps
A mixture of methyl 2-fluoroacetate (11.3 mg, 123 μmol, Eq: 1.5) and KOSiMe3 (21 mg, 164 μmol, Eq: 2) in Dioxane (1 ml) was stirred at room temperature over night. Trans-4-[2-(4-Benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexylamine hydrochloride (Intermediate A) (30 mg, 81.8 μmol), N,N-diisopropylethylamine (42.3 mg, 57.0 μl, 327 μmol, Eq: 4) and TBTU (39.4 mg, 123 μmol, Eq: 1.5) were added. Reaction mixture was stirred 4 h at room temperature. The reaction mixture was solved with sat NaHCO3 (1×10 mL) and extracted with dichloromethane (2×20 mL). The organic layers were dried over MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 10 g, 0% to 20% MeOH in dichloromethane) to yield the title compound as an off-white solid (21.3 mg, 66.7%), MS (ISP) m/z=391.2 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598357B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-0566a8f358414610984b94cc673c4691 |
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| Source note | uspto-grants-2013_12 |
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