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

Ethyl Acrylate → Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate

HRID 1754
Notes
Print preview

Reaction equation

HRID 1754 reaction equation
[OH:1][C:2]1[C:3](I)=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1.C([O-])(=O)C.[K+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:34]([O:38][CH2:39][CH3:40])(=[O:37])[CH:35]=[CH2:36]>CN(C=O)C.O.[Pd](Cl)Cl>[OH:1][C:2]1[C:3]([C:35](=[CH2:36])[C:34]([O:38][CH2:39][CH3:40])=[O:37])=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 8821Ethyl AcrylateHCID 11776TriphenylphosphineHCID 899572-Iodo-6-methylpyridin-3-olHCID 517044Potassium Acetate

Product 1

HCID 131720091Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate

Reagents, catalysts & solvents 3

HCID 24290
Palladium Chloride
Catalyst
HCID 962WaterSolvent
HCID 6228DimethylformamideSolvent

Conditions

Temperature
120 °C

Procedure

To a solution of 3-hydroxy-2-iodo-6-methylpyridine (1.175 g, 5.0 mmol) in DMF (9.5 ml) and water (0.5 ml) were added potassium acetate (1.23 g, 12.5 mmol), triphenylphosphine (105 mg, 0.40 mmol), palladium chloride (36 mg, 0.20 mmol) and ethyl acrylate (1.63 ml, 1.50 g, 15.0 mmol). The mixture was placed under nitrogen and heated at 120° C. for 1.5 h. The mixture was cooled, filtered from deposited palladium black, and added to water (100 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (2×25 ml) and with brine (25 ml), then dried over sodium sulphate and evaporated. This left a tan solid, the product (951 mg, 91%). mp 192°-195° C. (dec)

Workup

  1. temperatureThe mixture was cooled
  2. filtrationfiltered
  3. additionadded to water (100 ml)
  4. extractionThe product was extracted into ethyl acetate (3×30 ml)
  5. washThe combined extracts were washed with water (2×25 ml) and with brine (25 ml)
  6. dry with materialdried over sodium sulphate
  7. customevaporated
  8. waitThis left a tan solid

Sources & evidence

ORD record
ord-daea2679130c4e96a69efc91647c4537
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05726315

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes