HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267596Generated: November 3, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 58997967, compound
https://huagongshe.com/reaction/2267596
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2,5-Difluorobenzaldehyde | HCID 137663 | — |
| Reactant | Methyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetate | HCID 2734718 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58997967 | HCID 58997967 | 82% |
Reaction Steps
A stirred solution of N-(benzyloxycarbonyl)-α-phosphonoglycine trimethyl ester (6.1 g) and 2,5-difluorobenzaldehyde (2.0 g) in dry dichloromethane (60 mL), was treated dropwise with a solution of DBU (2.5 mL) in dichloromethane (20 mL). The mixture was stirred at room temperature for 2 h, then was concentrated to approximately 20 mL and partitioned between ethyl acetate (150 mL) and 1N hydrochloric acid (50 mL). The organic extract was collected, consecutively washed with 1N hydrochloric acid, water, saturated aqueous sodium bicarbonate, and brine, dried (sodium sulfate), filtered and evaporated. The crude product (6.5 g) was purified by flash chromatography (20% ethyl acetate/hexanes) to yield the title compound (4.0 g, 82%). 1H NMR (300 MHz, CDCl3) δ 3.85 (s, 3H), 5.10, (s, 2H), 6.60 (bs, 1H), 6.9-7.1 (m, 2H), 7.21 (m, 1H), 7.2-7.3 (m, 6H). MS APCI, m/z=348 (M+1). LC/MS: 2.53 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858776B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-217e547b60404b1d948d4f73f0339a0c |
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| Source note | uspto-grants-2010_12 |
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