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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888310Generated: October 31, 2026

Benzyl Alcohol → HCID 67303962, compound

https://huagongshe.com/reaction/888310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSulfuric AcidHCID 1118—
Reactant(R)-3-PyrrolidinolHCID 2759337—
ReactantHCID 16047991HCID 16047991—
SolventIsopropanolHCID 3776—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 67303962HCID 673039627%

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 %) as impurities was dissolved in 9 ml of isopropanol, followed by adding 240 mg of sulfuric acid under ice cold conditions. 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 was heated to 40° C., 209 mg of isopropanol was added and the concentrate was dissolved completely. After the solution was gradually cooled to 22° C., 207 mg of hexane was added, and then a seed crystal was further added, and the deposited crystal was filtered under reduced pressure. The resultant wet crystal was dried under reduced pressure, thereby obtaining 75 mg of dry crystal of (R)-3-benzyloxypyrrolidine sulfate (yield of 7%, purity of 99.9%). 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-957d96bd69e140bf8e23ad02b837a064
Source noteuspto-grants-2012_08