Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | (R)-3-Pyrrolidinol | HCID 2759337 | — |
| Reactant | HCID 16047991 | HCID 16047991 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67305675 | HCID 67305675 | 59% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247578B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-1503585d8cd8432f8536aee937d8a1f2 |
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| Source note | uspto-grants-2012_08 |
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