HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175761Generated: October 27, 2026
Cyanomethylenetributylphosphorane → tert-butyl(9aS)-3-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)hexahydropyrazino[2,1-c][1,4]oxazine-8(1H)-carboxylate
https://huagongshe.com/reaction/2175761
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanomethylenetributylphosphorane | HCID 4622928 | — |
| Reactant | tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate | HCID 71271745 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | tert-butyl(9aS)-3-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)hexahydropyrazino[2,1-c][1,4]oxazine-8(1H)-carboxylate | HCID 86727024 | — |
Reaction Steps
tert-Butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate (3.3 g, 8.4 mmol) and cyanomethylene tri-n-butylphosphorane (3.65 g, 15.1 mmol) were dissolved in 30 mL of benzene, the solution was degassed, and then heated to 100° C. for 3 h. LC-MS showed the product peak (M+1=389). The reaction mixture was cooled and evaporated to dryness. The residue was purified by MPLC through a 330 g Redi-sep column and eluted with a 15% acetone/85% hexane mixture to yield a cis-trans mixture of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062070B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-cc71e64ae94c4d188310e22a9758c01f |
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| Source note | uspto-grants-2015_06 |
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