Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Methylcyclobutane-1-carbaldehydeHCID 53782318—
ReactantN-(benzyloxycarbonyl)-alpha-phosphonoglycine methyl esterHCID 66895383—
SolventDichloromethaneHCID 6344—
ProductHCID 66893747HCID 6689374738%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-ba0029940a7641e184d408142a9d0075
Source noteuspto-grants-2010_06