HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736918Generated: October 27, 2026
Hydrochloric Acid → HCID 22184582, compound
https://huagongshe.com/reaction/736918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-amino-3-chloro-5-(trifluoromethyl)benzoic Acid | HCID 4643549 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22184582 | HCID 22184582 | 33.8% |
Reaction Steps
69.56 g (0.43 mol) CDI were added to a solution of 93.4 g (0.39 mol) 4-amino-3-chloro-5-trifluoromethyl-benzoic acid (described in Arzneim.-Forsch. 1984, 34(11A), 1612-1624) in 1 L THF and the mixture was stirred for 1 h at 40° C. The reaction mixture was then carefully added to a solution of 51.4 g (1.36 mol) NaBH4 in 450 mL of water at RT under a nitrogen atmosphere and with cooling. The mixture was stirred for 2 h at RT, combined with 500 mL water and 300 mL semiconc. HCl, stirred for another hour and then exhaustively extracted with EtOAc. The combined org. phases were dried over Na2SO4 and evaporated down i. vac. The oil remaining was combined with 500 mL PE and stirred while cooling with ice. The precipitate was suction filtered, washed with PE and dried. 29.7 g of the desired product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595312B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-88b81ef181254587abfa2ba7977e3706 |
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| Source note | uspto-grants-2009_09 |
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