Sodium Carbonate → Biotin

HRID 569586Notes

Reaction equation

HRID 569586 reaction equation
S=[C:2]([CH2:6][CH2:7][CH2:8][C@H:9]1[C@@H:17]2[C@@H:12]([NH:13][C:14]([NH:16]2)=[O:15])[CH2:11][S:10]1)[C:3](=[O:5])[OH:4].BrC(O)C.C(=O)([O-])[O-].[Na+].[Na+]>COCCOCCOC>[OH:5][C:3]([CH2:2][CH2:6][CH2:7][CH2:8][C@H:9]1[C@@H:17]2[C@@H:12]([NH:13][C:14]([NH:16]2)=[O:15])[CH2:11][S:10]1)=[O:4]

Participants

5

Reactant 3

HCID 10340Sodium CarbonateHCID 14202443Ethanol, 1-bromo-HCID 22827484HCID 22827484, compound

Product 1

HCID 171548BiotinYield 62%

Reagents, catalysts & solvents 1

HCID 8150DiglymeSolvent

Procedure

A diglyme solution (3 ml) containing dl-thioxobiotin (255 mg. 0.981 mol) and bromoethanol (140 μl, 1.98 mmol) was allowed to reflux (150°) for 2.5 hours. The solution was cooled, dilute sodium carbonate (50 ml) was added, and the solution was extracted with hexane (50 ml). The pH of the aqueous phase was adjusted to 1.5 with 6N HCL and extracted with ethyl acetate (4×100 ml). The ethyl acetate extract was dried over magnesium sulfate, filtered and concentrated in vacuo to give 148 mg (62%) of crude biotin, mp 220°-223° C. which was recrystallized from water IR (KBr) 3279, 2899, 1724; NMR (d, DMSO) 0.76-1.95 (6H, m, C--CH2), 2.00-2.40 (2H, t, CH2 --CO), 2.70-2.98 (1H, m, CH2S) 3.00-3.54 (2H, m, CH2S, CHS) 4.00-4.44 (2H, m, CHN), 6.44 (1H, bs, NH), 6.55 (1H, bs, NH), 11.8-12.4 (1H, bs, OH). Analysis calculated for C10H16O3N2S: C, 49.18; H, 6.56; N, 11.48; Found: C, 49.30; H, 6.23; N, 11.37. Mass spectrum: calculated: 244.0880, found: 244.0925.

Workup

  1. temperatureto reflux (150°) for 2.5 hours
  2. temperatureThe solution was cooled
  3. extractionthe solution was extracted with hexane (50 ml)
  4. extractionextracted with ethyl acetate (4×100 ml)
  5. extractionThe ethyl acetate extract
  6. dry with materialwas dried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-7290c58d46454912b69e62f727cc8917
Source dataset
uspto-grants-1988_03
Patent number
US04732988

Reaction notes

Loading…