HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028883Generated: October 30, 2026
CID 406 → tert-Butyl[2,2-Dimethyl-5-(4-octanoylstyryl)-1,3-dioxan-5-yl]carbamate
https://huagongshe.com/reaction/1028883
Participants
| Role | Name | HCID | Charge |
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| Reactant | CID 406 | HCID 406 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl (5-formyl-2,2-dimethyl-1,3-dioxan-5-yl)carbamate | HCID 24754730 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl[2,2-Dimethyl-5-(4-octanoylstyryl)-1,3-dioxan-5-yl]carbamate | HCID 123791953 | — |
Reaction Steps
A mixture of the Wittig reagent (23, X═O) or the phosphonate (0.3 mmol), aldehyde (24) (0.33 mmol), and K2CO3 (0.9 mmol) in a mixture of THF (3 ml) and DMF (1 ml) was heated at 70-75° C. under TLC and HPLC monitoring. After completion of the reaction, THF was evaporated and the reaction mixture was quenched with water and then extracted with ethyl acetate. The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated. After purification, the title compound (26) was recovered as white solid with 72% yield, mp 82-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735627B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-51e2f1efc7c34241b66e8e50c59a693e |
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| Source note | uspto-grants-2014_05 |
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