Hydrochloric Acid → Tryptophan--hydrogen chloride (1/1)

HRID 1728910Notes

Reaction equation

HRID 1728910 reaction equation
[NH2:1][C@H:2]([C:13]([OH:15])=[O:14])[CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1.[ClH:16].[Cl-].[Na+]>>[ClH:16].[NH2:1][C@H:2]([C:13]([OH:15])=[O:14])[CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1

Participants

4

Conditions

Temperature
15 °C

Procedure

The pH of 30 l of L-tryptophan fermentation broth was adjusted to 3.5 with 35% hydrochloric acid. After the cells were removed from the broth by centrifugation, the solution was concentrated at a temperature of 60° C. under reduced pressure, until the concentration of L-tryptophan reached 180 g/l. Next, 3.5 equivalents of 35% hydrochloride acid and 3 equivalents of sodium chloride (both relative to the amount of L-tryptophan) were added to the slurry, while keeping the concentrated slurry at 50° C. After cooling to 15° C. overnight, the crystals were separated with a centrifuging machine, and were washed with water. The crystals were dried at 60° C. for 2 hours under reduced pressure to give 156 g of L-tryptophan hydrochloride crystals. The L-tryptophan hydrochloride crystals thus obtained had a purity of 95.7%.

Workup

  1. customAfter the cells were removed from the broth by centrifugation
  2. concentrationthe solution was concentrated at a temperature of 60° C. under reduced pressure, until the concentration of L-tryptophan
  3. customat 50° C
  4. customthe crystals were separated with a centrifuging machine
  5. washwere washed with water
  6. customThe crystals were dried at 60° C. for 2 hours under reduced pressure

Sources & evidence

ORD record
ord-42e2bbac1e584d8db60f4275de605618
Source dataset
uspto-grants-1994_07
Patent number
US05329014

Reaction notes

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