Benzyl Alcohol → HCID 67305675, compound

HRID 1009823Notes

Reaction equation

HRID 1009823 reaction equation
[CH2:1]([O:8][C@@H:9]1[CH2:13][CH2:12][NH:11][CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O[C@@H]1CCNC1.C(O)C1C=CC=CC=1.[BrH:28]>C(O)(C)C.C(OCC)(=O)C>[BrH:28].[CH2:1]([O:8][C@@H:9]1[CH2:13][CH2:12][NH:11][CH2:10]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

7

Conditions

Temperature
40 °C

Procedure

1.0 g of a concentrate containing (R)-3-benzyloxypyrrolidine obtained in Example 15 (purity of 86.6%) containing (R)-3-hydroxypyrrolidine (content of 0.12 wt %) and benzyl alcohol (content of 1.9 wt %) were contained as impurities were dissolved in 9 ml of isopropanol, followed by adding 0.82 g of 48% hydrobromic acid under ice cold condition. After stirring for a while, the mixture was concentrated and dried under reduced pressure, thereby obtaining a concentrate. After the concentrate was dispersed in 4.0 g of ethyl acetate and heated to 40° C. for complete dissolution, the solution was gradually cooled to 22° C. The deposited crystal was filtered under reduced pressure, and the resultant wet crystal was dried under reduced pressure, thereby obtaining 0.74 g of dry crystal of (R)-3-benzyloxypyrrolidine hydrobromide (yield of 59%, purity of 100.0%). Each of (R)-3-hydroxypyrrolidine and benzyl alcohol in the crystal was 0.01 wt % or less.

Workup

  1. concentrationthe mixture was concentrated
  2. customdried under reduced pressure
  3. customobtaining a concentrate
  4. temperaturethe solution was gradually cooled to 22° C
  5. filtrationThe deposited crystal was filtered under reduced pressure
  6. customthe resultant wet crystal was dried under reduced pressure

Sources & evidence

ORD record
ord-1e5486ee95024125a53a44ba2214b087
Source dataset
uspto-grants-2011_07
Patent number
US07973176B2

Reaction notes

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