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Hydrochloric Acid → Methyl 6,6,6-trifluoro-5-hydroxynorleucinate hydrochloride

HRID 1844199
Notes
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Reaction equation

HRID 1844199 reaction equation
[ClH:1].[F:2][C:3]([F:14])([F:13])[CH:4]([OH:12])[CH2:5][CH2:6][C@@H:7]([C:9]([OH:11])=[O:10])[NH2:8].[CH3:15]O>>[ClH:1].[F:2][C:3]([F:13])([F:14])[CH:4]([OH:12])[CH2:5][CH2:6][C@@H:7]([C:9]([O:11][CH3:15])=[O:10])[NH2:8]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 90115630Rac-6,6,6-trifluoro-5-hydroxynorleucine

Product 1

HCID 86718222Methyl 6,6,6-trifluoro-5-hydroxynorleucinate hydrochloride

Procedure

1.4 ml of saturated hydrochloric acid in methanol were added to 150 mg (0.7 mmol) of rac-6,6,6-trifluoro-5-hydroxynorleucine (stereoisomer mixture), and the mixture was stirred under reflux overnight. The reaction solution was concentrated, another 1.5 ml of saturated hydrochloric acid in methanol were added and the mixture was stirred under reflux overnight. The reaction solution was concentrated and the residue was dried under high vacuum. This gave 185 mg (99% of theory) of the target compound.

Workup

  1. temperatureunder reflux overnight
  2. concentrationThe reaction solution was concentrated
  3. additionanother 1.5 ml of saturated hydrochloric acid in methanol were added
  4. stirringthe mixture was stirred
  5. temperatureunder reflux overnight
  6. concentrationThe reaction solution was concentrated
  7. customthe residue was dried under high vacuum

Sources & evidence

ORD record
ord-fccb93fb15a0462990f4a2d05e95feab
Source dataset
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08946215B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes