HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Potassium Bromide → 2-Bromohexanoic acid, (S)-

HRID 52803
Notes
Print preview

Reaction equation

HRID 52803 reaction equation
[Br-:1].[K+].N[C@@H:4]([C:9]([OH:11])=[O:10])[CH2:5][CH2:6][CH2:7][CH3:8].N([O-])=O.[Na+]>S(=O)(=O)(O)O>[Br:1][C@@H:4]([CH2:5][CH2:6][CH2:7][CH3:8])[C:9]([OH:11])=[O:10]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 253877Potassium BromideHCID 456468Norleucine, D-(-)-HCID 23668193Sodium Nitrite

Product 1

HCID 69944632-Bromohexanoic acid, (S)-

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Conditions

Temperature
-10 °C

Procedure

Potassium bromide (15.9 g., 133 mmol.) was added to a stirred solution of D-norleucine (5.0 g., 38 mmol.) in 2.5N sulfuric acid (77 ml.) at room temperature. The reaction mixture was cooled to -10° C. and solid sodium nitrite (3.94 g., 57 mmol.) was added portionwise, maintaining the temperature between -10° and -5° C. After addition was complete, the foamy reaction was stirred for 1 hour and then warmed to room temperature and stirred for another hour. The reaction mixture was then extracted twice with ether, the ether extracts were washed once with water, dried (magnesium sulfate), filtered and evaporated to give 3.3 g. of crude title product.

Workup

  1. temperaturemaintaining the temperature between -10° and -5° C
  2. additionAfter addition
  3. customthe foamy reaction
  4. temperaturewarmed to room temperature
  5. stirringstirred for another hour
  6. extractionThe reaction mixture was then extracted twice with ether
  7. washthe ether extracts were washed once with water
  8. dry with materialdried (magnesium sulfate)
  9. filtrationfiltered
  10. customevaporated
  11. customto give 3.3 g

Sources & evidence

ORD record
ord-7f620ed86bf7481ebc5ee6448c6f51f0
Source dataset
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05616775

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes