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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725122Generated: November 1, 2026

1-Octanol → HCID 67653950, compound

https://huagongshe.com/reaction/725122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-OctanolHCID 957—
ReactantPyridineHCID 1049—
ReactantHCID 86751842HCID 86751842—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 67653950HCID 6765395054%

Reaction Steps

0.66 g (5 mmol) of 1-octanol was dropwise added to the solution of 1.5 g (3.2 mmol) of 6-{N-[2,5-di(benzyloxy)benzoyl]amino}hexanoyl chloride in 15 ml of anhydrous acetonitrile and 0.29 g (3.7 mmol) of anhydrous pyridine during 5 minutes under cooling and stirring at 0°-5° C. The reaction mixture was stirred at room temperature for 10 hours, then evaporated under reduced pressure to dryness at a temperature below 50° C. The residue obtained was dissolved in 40 ml of ether and was successively washed with water, 2% sodium hydroxide solution and finally with water, then dried and evaporated under reduced pressure. The residue was purified on a silicagel column by using ethyl acetate as eluent to give 0.96 g (54%) of the aimed compound, m.p.: 48°-50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705529
Source datasetuspto-grants-1998_01
ORD IDord-b172fb8cfcea49bab4f7a2fbb32f36b8
Source noteuspto-grants-1998_01