HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324057Generated: October 30, 2026
Hydrochloric Acid → HCID 22237691, compound
https://huagongshe.com/reaction/324057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22237421 | HCID 22237421 | — |
| Reactant | HCID 22237463 | HCID 22237463 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 22237691 | HCID 22237691 | 85.2% |
Reaction Steps
A stirring solution of 3,5-bis-(m-trifluoromethylphenyl)-4-hydroxybenzoic acid (0.800 g, 1.87 mmol) in SOCl2 (10 mL) was heated at reflux for 1.5 h, then cooled and concentrated in vacuo. The acid chloride was dried in vacuo overnight. The acid chloride was dissolved in CH2Cl2 (10 mL) and added to a solution of 6-(4-benzyloxy-benzyloxy)hexylamine (0.765 g, 2.44 mmol) and triethylamine (0.92 mL, 6.54 mmol) in CH2Cl2 (10 mL) at 0° C. After stirring for 4 h at 0° C., 1.0 N HCl was added, and the mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried (MgSO4), and concentrated to give 1.15 g (85%) of the amide as an oil: 1H NMR (DMSO-d6) δ9.30 (s, 1H), 8.44 (t, 1H), 7.94-7.70 (m, 10H), 7.41 (m, 4H), 7.20 (d, 2H), 6.95 (d, 2H), 5.08 (s, 2H), 4.35 (s, 2H), 3.42-3.20 (m, 4H), 1.50 (m, 4H), 1.32 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214877B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-2a9ec81d76674ce2b93eaec2e76ced0c |
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| Source note | uspto-grants-2001_04 |
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