HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612446Generated: October 30, 2026
Potassium Carbonate → (R)-1-(2-(6,11-dihydrodibenzo[b,e]thiepin-11-ylidene)-1-ethyl)-3-piperidinecarboxylic acid ethyl ester hydrogen oxalate
https://huagongshe.com/reaction/612446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (R)-(-)-Ethyl Nipecotate Tartrate | HCID 2733695 | — |
| Reactant | 11-(2-Bromoethylidene)-6,11-dihydrodibenzo[b,e]thiepine | HCID 53962804 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-1-(2-(6,11-dihydrodibenzo[b,e]thiepin-11-ylidene)-1-ethyl)-3-piperidinecarboxylic acid ethyl ester hydrogen oxalate | HCID 69947848 | 86% |
Reaction Steps
To a solution of 11-(2-bromoethylidene)-6,11-dihydrodibenzo[b,e]thiepine (4.43 g, 0.014 mol, Coll.Czech.Chem.Comm. 52, 1566 (1987)) in N,N-dimethylformamide (75 ml), potassium carbonate (19.3 g, 0.14 mol) and (R)-3-piperidinecarboxylic acid ethyl ester tartrate (6.43 g, 0.0209 mol) were added and the mixture was stirred at 70° C. for 6 h. The reaction mixture was diluted with benzene (300 ml), the solid was filtered off and the filtrate was washed with water (5×80 ml). The benzene solution was dried (MgSO4) and the solvent removed in vacuo. The oily residue (6.83 g) was dissolved in acetone and treated with a solution of oxalic acid in ethanol. The solid was isolated and the crude hydrogen oxalate (5.8 g) was recrystallised from a mixture of 96% ethanol and ether to yield 5.81 g (86%) of (R)-1-(2-(6,11-dihydrodibenzo[b,e]thiepin-11-ylidene)-1-ethyl)-3-piperidinecarboxylic acid ethyl ester hydrogen oxalate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06004983 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-f9a4d39ae7a342798ae46dd0db2e2d0a |
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| Source note | uspto-grants-1999_12 |
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