HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535332Generated: October 30, 2026
Hydrochloric Acid → HCID 86718439, compound
https://huagongshe.com/reaction/535332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86718440 | HCID 86718440 | — |
| Catalyst | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86718439 | HCID 86718439 | 90.9% |
Reaction Steps
To a solution of 3-Methoxymethylene-9-thia-bicyclo[3.3.1]nonane (2.50 g, 13.56 mmol) in THF (35 ml) were added water (7 ml) and a 4M solution of HCl (6.78 ml, 27.10 mmol) and the reaction mixture was stirred for 16 hrs at 55° C. The reaction mixture was quenched with a saturated aqueous solution of NaHCO3, ethyl acetate was added and extracted with ethyl acetate. The organic phases were combined, washed with brine, dried using Na2SO4, filtered and concentrated in vacuo. The remaining oil was dissolved in THF/MeOH 1/1 (60 ml), DBU (0.146 g, 0.14 ml, 0.957 mmol) was added and the solution was stirred at RT for 1 hr. Ethyl acetate (150 ml), the reaction mixture was neutralized using a solution of 0.5 M HCl and extracted with ethyl acetate. The combined organic phases were washed with brine, dried using Na2SO4 and concentrated in vacuo. The crude product was purified by silica gel column chromatography (eluting with a gradient of hexanes:ethyl acetate 100:0 to 75:25) yielding the title intermediate (2.21 g, 12.33 mmol, 64%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859535B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-e5ff97e633d742fa8fe6444c2ab5d216 |
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| Source note | uspto-grants-2014_10 |
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