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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535332Generated: October 30, 2026

Hydrochloric Acid → HCID 86718439, compound

https://huagongshe.com/reaction/535332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 86718440HCID 86718440—
Catalyst1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86718439HCID 8671843990.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859535B2
Source datasetuspto-grants-2014_10
ORD IDord-e5ff97e633d742fa8fe6444c2ab5d216
Source noteuspto-grants-2014_10