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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888308Generated: October 30, 2026

Benzyl Alcohol → HCID 67305675, compound

https://huagongshe.com/reaction/888308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrogen BromideHCID 260—
Reactant(R)-3-PyrrolidinolHCID 2759337—
ReactantHCID 16047991HCID 16047991—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductHCID 67305675HCID 6730567559%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247578B2
Source datasetuspto-grants-2012_08
ORD IDord-1503585d8cd8432f8536aee937d8a1f2
Source noteuspto-grants-2012_08