HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442905Generated: October 30, 2026
Potassium Carbonate → HCID 54533967, compound
https://huagongshe.com/reaction/442905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 6-bromohexanoate | HCID 117544 | — |
| Reactant | HCID 54501570 | HCID 54501570 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54533967 | HCID 54533967 | 100.3% |
Reaction Steps
3-Benzyloxy-5-methyl-1-(2-trifluoromethylphenylsulfonylamino)benzene (550 mg, 1.3 mmol), as prepared in the preceding step, ethyl 6-bromohexanoate (290 mg, 1.3 mmol), and K2CO3 (1.0 g) were mixed in N,N-dimethylformamide (10 mL). The mixture was heated to 60° C. and stirred for 12 h. The solid was removed by filtration, and the filtrate was evaporated under high vacuum. The residue was dissolved in ethyl acetate (100 mL), washed with saturated aqueous NaHCO3 (2×50 mL) and brine (2×50 mL), and dried over Na2SO4. The solvent was evaporated in vacuo to give the title compound as a pale red oil (735 mg, 100%) which was directly used for the next step. 1H-NMR (300 MHz, CDCl3) δ 7.85 (d, J=7.7 Hz, 1 H), 7.71 (d, J=7.8 Hz, 1 H), 7.60 (t, J=7.7 Hz, 1 H), 7.47 (t, J=7.7 Hz, 1 H), 7.37 (m, 5 H), 6.71 (s, 1 H), 6.53 (s, 1 H), 6.51 (s, 1 H), 4.95 (s,2H), 4.11 (q, J=7.1 Hz, 2 H),3.66(t,J=7.0 Hz, 2 H), 2.25 (t, J=7.4 Hz, 2 H), 2.23 (s, 3 H), 1.33-1.62 (m, 6 H), 1.24 (t, J=7.1 Hz, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891909 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-5c8949ba7e5b49b2938cb292822b5968 |
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| Source note | uspto-grants-1999_04 |
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