Methanol → O-benzyl-L-tyrosine

HRID 1354909Notes

Reaction equation

HRID 1354909 reaction equation
[NH2:1][C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.CO.[CH2:16](Br)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>[OH-].[Na+].S([O-])([O-])(=O)=O.[Cu+2]>[NH2:1][C@@H:2]([CH2:3][C:4]1[CH:5]=[CH:6][C:7]([O:10][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:8][CH:9]=1)[C:11]([OH:13])=[O:12]

Participants

6

Reactant 3

HCID 887MethanolHCID 6057L-TyrosineHCID 7498Benzyl Bromide

Product 1

HCID 725701O-benzyl-L-tyrosine

Reagents, catalysts & solvents 2

HCID 24462Copper SulfateCatalystHCID 14798Sodium HydroxideSolvent2×

Conditions

Temperature
60 °C

Procedure

To a solution of L-tyrosine of the formula (21) (18.1 g) in 2N NaOH solution (115 ml), copper sulphate solution (12.5 g of CuSO4 in 50 ml of water) was added and heated at 60° C. for 1.5 h. The reaction mixture was cooled to room temperature and methanol (350 ml) and 2N NaOH (12.5 ml) was added and then benzyl bromide (12 ml) was added drop wise. The reaction mass was allowed to warm to room temperature. The precipitate was filtered and washed to give the title compound as white to off-white solid (18.5 g, 66.8%) (Ref. Bodansky & Bodansky pp50).

Workup

  1. temperatureThe reaction mixture was cooled to room temperature
  2. temperatureto warm to room temperature
  3. filtrationThe precipitate was filtered
  4. washwashed

Sources & evidence

ORD record
ord-a11ef0aa35814a638cd532d27102dfac
Source dataset
uspto-grants-2007_05
Patent number
US07223881B2

Reaction notes

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