Reaction #1121783

ord-14f1e1cffcb449c09da97e767783b332

Reaction equation

[H-].[Na+]
Sodiumhydride
OCc1ccccc1
Benzylalkohol
OCc1ccccc1
benzylalkohol
Clc1ncnc2nc[nH]c12
6-chloropurine
c1ccc(COc2ncnc3nc[nH]c23)cc1
6-Benzyloxypurine

Solvents

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherhas reached room temperature
  2. 2
    Other6-Benzyloxypurine was precipitated by the addition of acetic acid (4.6 ml) and diethylether (550 ml)
  3. 3
    OtherThe precipitate was separated by filtration (11.72 g)
  4. 4
    OtherRecrystallization from ether
  5. 5
    Othergave (4.78 g; 65.4%)
  6. 6
    Other170-172° C.

Procedure

Sodiumhydride (60% Dispersion in mineral oil; 3.23 g; 80 mmol) was slowly added to Benzylalkohol (30 ml; 34.7 mmol). After the addition of more benzylalkohol (10 ml) and 6-chloropurine (5.36 g). The reaction mixture was heated to 100° C. for 4 hours. When the reaction mixture has reached room temperature, water (1 ml) was slowly added. 6-Benzyloxypurine was precipitated by the addition of acetic acid (4.6 ml) and diethylether (550 ml). The precipitate was separated by filtration (11.72 g). Recrystallization from ether gave (4.78 g; 65.4%). Melting point 175-177° C. (litt. 170-172° C.)[Ramazaeva N., 1989 #473] 1H-NMR (DMSO-d6): 8.53 (1H, s); 8.39 (1H, s); 7.54-7.35 (5H, m); 5.62 (2H, s).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08546309B2uspto-grants-2013_10