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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073299Generated: October 30, 2026

1-Octanol → HCID 54534880, compound

https://huagongshe.com/reaction/1073299

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-OctanolHCID 957—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—
SolventDichloromethaneHCID 6344—
Solvent4-PyrrolidinopyridineHCID 75567—
ProductHCID 54534880HCID 54534880—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

13.2 parts by weight of 1-carbobenzoxypiperidine-4-carboxylic acid are dissolved in 150 parts by volume of methylene chloride, 8 parts by volume of n-octanol and 0.7 part by weight of 4-pyrrolidinopyridine are added, and the mixture is cooled to 0 to 5° C. 12.0 parts by weight of dicyclohexylcarbodiimide are added, and the mixture is stirred at 5° C. for 2 hours and at room temperature for 4 hours. The mixture is left to stand overnight, the precipitated dicyclohexylurea is filtered off with suction (11.3 parts by weight), the solvent is stripped off in vacuo, the residue is stirred with diisopropyl ether in order to remove residual dicyclohexylurea and filtered, and the solvent is stripped off. 21 parts by weight of an oily residue are obtained. The residue is chromatographed on 1070 parts by weight of silica gel using CH2Cl2 /5% of methanol. 9.8 parts by weight of the compound (A) are obtained as an oil. ##STR42## 4-decyloxyphenoxy(4-benzoyl) chloroformate =(B)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968798
Source datasetuspto-grants-1990_11
ORD IDord-f791ce0f76aa475ba378c32a0c180bd0
Source noteuspto-grants-1990_11