HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19299Generated: October 26, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 66893747, compound
https://huagongshe.com/reaction/19299
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-Methylcyclobutane-1-carbaldehyde | HCID 53782318 | — |
| Reactant | N-(benzyloxycarbonyl)-alpha-phosphonoglycine methyl ester | HCID 66895383 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66893747 | HCID 66893747 | 38% |
Reaction Steps
In a round bottom flask under argon was placed N-(benzyloxycarbonyl)-α-phosphonoglycine methyl ester (3.04 g, 9.16 mmol) in dichloromethane (10 mL) and cooled to 0° C. This mixture was treated dropwise with 1,8-diazabicyclo[5.4.0]undec-7-ene (1.20 mL, 7.94 mmol) and stirred at 0° C. for 20 min. A solution of 3-methyl-cyclobutanecarbaldehyde (600 mg, 6.11 mmol) in dichloromethane (5 mL) was then added. After the addition was complete the reaction was warmed to 25° C. and stirred overnight. The mixture was then concentrated in vacuo and dissolved in ethyl acetate (100 mL). The ethyl acetate layer was washed with a saturated aqueous ammonium chloride solution (2×50 mL), a saturated aqueous solution of sodium chloride (50 mL), dried over sodium sulfate and concentrated in vacuo with silica gel (3 g). Purification by Biotage flash chromatography (40M column, 20% ethyl acetate/hexanes) afforded (Z)-2-benzyloxycarbonylamino-3-(3-methyl-cyclobutyl)-acrylic acid methyl ester (693 mg, 38%) as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-ba0029940a7641e184d408142a9d0075 |
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| Source note | uspto-grants-2010_06 |
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