HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989145Generated: October 30, 2026
Potassium Carbonate → HCID 22860743, compound
https://huagongshe.com/reaction/989145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 6-Bromohexanoate | HCID 4170292 | — |
| Reactant | HCID 10811257 | HCID 10811257 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22860743 | HCID 22860743 | 65% |
Reaction Steps
To a solution of 0.259 g (0.64 mmol) of 2-(S)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(R)-phenylmorpholine (from example 33) in 2 mL of DMF were added 0.16 g (0.77 mmol) of methyl 6-bromohexanoate, 0.155 g (1.12 mmol) of K2CO3 and 2 crystals of nBu4NI. The resulting solution was heated in a 60° C. bath for 36 h, at which time a tlc indicated incomplete reaction. The bath temperature was raised to 100° C. After 3 h the reaction mixture was cooled and diluted with EtOAc. The EtOAc solution was washed with water (2×), brine and dried over Na2SO4. The filtrate was concentrated and the residue was chromatographed using 30% EtOAc/hexane to isolate 220 mg (65%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06638930B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-509e95ea48a1426cb1ca40ffab6d4586 |
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| Source note | uspto-grants-2003_10 |
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