HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003743Generated: October 31, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 18798270, compound
https://huagongshe.com/reaction/1003743
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Reactant | 3,4-Difluorophenylacetyl chloride | HCID 14618085 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18798270 | HCID 18798270 | 3.4% |
Reaction Steps
3,4-Difluorophenylacetic acid (3.61 g, 20.9 mmol) in oxalyl chloride (7.31 ml, 83.8 mmol) was refluxed for 4 hours. The solution was cooled to room temperature, concentrated under reduced pressure to give 3,4-difluorophenylacetyl chloride which was used without purification. To a well stirred solution of 3,4-difluorophenylacetyl chloride (2.21 g, 11.59 mmol) in THF (10 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (3.47 mL, 23.18 mmol) at room temperature and the solution was stirred for five minutes. Then methylisocyanoacetate (1.55 mL, 11.59 mmol) was added over a three minute period to the reaction mixture. After stirring for 18 hours at room temperature, the reaction mixture was partitioned between ether (100 mL) and water (50 mL). The organic layer was washed with 1N HCl (10 mL), water (15 mL) and saturated solution of sodium bicarbonate (15 mL), and dried over sodium sulfate. The solution was then filtered and concentrated. The residue was chromatographed (hexanes:EtOAc, 3:2) to yield 100 mg (3.4%) of the product; 1H-NMR (CDCl3) δ3.89 (s, 3H), 6.98 (s, 2H), 7.00-7.09 (m, 3H), 7.73 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046331 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-9be2a64fff1e4d94916d8e3db22c2818 |
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| Source note | uspto-grants-2000_04 |
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