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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyanideHCID 5975—
ReactantSodium CyanideHCID 8929—
ReactantMethyl trifluoromethyl ketoneHCID 9871—
Product3,3,3-Trifluoro-2-hydroxy-2-methylpropanenitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06261830B1
Source datasetuspto-grants-2001_07
ORD IDord-ef0a6f05644a465c844e764e853b34e9
Source noteuspto-grants-2001_07