HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213370Generated: October 31, 2026
Ethyl difluoroacetate → HCID 21957343, compound
https://huagongshe.com/reaction/2213370
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl difluoroacetate | HCID 9961 | — |
| Reactant | HCID 21051178 | HCID 21051178 | — |
| Product | HCID 21957343 | HCID 21957343 | — |
Reaction Steps
The compound is prepared from {3-[4-(4-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamic acid tert-butyl ester (250 mg, 0.64 mmol) and ethyl difluoroacetate (120 mg, 0.96 mmol) following the method described for Example 5 (using ethyl difluoroacetate as starting agent). The product is purified by silica gel column chromatography (eluent 1% MeOH in EtOAc) and recrystallized from MeOH to provide the title compound. MS (m/z): 366 [M+1]. 1H NMR (300 MHz, DMSO) δ 9.16 (t, J=5.8 Hz, 1H), 7.73 (d, J=8.0 Hz, 1H), 7.53 (d, J=9.1 Hz, 2H), 7.28 (d, J=9.1 Hz, 2H), 6.24 (t, J=53.0 Hz, 1H), 4.98 (d, J=7.7 Hz, 1H), 4.80–4.75 (m, 1H), 4.14 (t, J=9.1 Hz, 1H), 3.97–3.92 (m, 2H), 3.76 (dd, J=6.3 and 9.1 Hz, 1H), 3.52 (t, J=5.5 Hz, 2H), 2.47 (t, J=7.1 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105547B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-92aa20dab29647828b49da118935553a |
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| Source note | uspto-grants-2006_09 |
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