HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384783Generated: October 31, 2026
Hydrochloric Acid → 3,3,3-Trifluoro-2-hydroxy-2-methylpropanenitrile
https://huagongshe.com/reaction/1384783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyanide | HCID 5975 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Product | 3,3,3-Trifluoro-2-hydroxy-2-methylpropanenitrile | HCID 274400 | — |
Reaction Steps
In Scheme 2, 1,1,1-trifluoroacetone (1) is reacted with a cyanide such as sodium cyanide in the presence of an acid such as hydrochloric acid to form racemic 3,3,3-trifluoro-2-hydroxy-2-methylpropanenitrile (2). The racemic 3,3,3-trifluoro-2-hydroxy-2-methylpropanenitrile (2) is then hydrolyzed with, for example, hydrochloric acid or sulfuric acid to provide racemic 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (3). Racemic (3) is then selectively crystallized with a resolving agent such as (lR,2S)-norephedrine (4) to form a salt (5) which may be recrystallized to diastereomeric purity. The purified salt (6) contains (S)-3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (7). (S)-3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acid (7) after liberation from the salt is reacted with 4-aminobenzophenone (8) and SOCl2 using an organic base such as triethylamine or Hunig's base to form (S)-(−)-N-(4-benzoylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide (9), which can then be purified by recrystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06261830B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-ef0a6f05644a465c844e764e853b34e9 |
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| Source note | uspto-grants-2001_07 |
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