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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403692Generated: October 29, 2026

Water → HCID 22412626, compound

https://huagongshe.com/reaction/403692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,6-HexanediolHCID 12374—
Reactant1-IodopropaneHCID 33643—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDichloromethaneHCID 6344—
ProductHCID 22412626HCID 2241262625%

Reaction Conditions

Temperature75 °C

Reaction Steps

a 500-mL, one-necked, round-bottom flask equipped with a magnetic stirrer was charged with 1,6-hexanediol (6.00 g), potassium tert-butoxide (5.413 g) at room temperature. The reaction mixture was stirred for one hour, and then 1-iodopropane (8.63 g) was added. The reaction mixture was heated to 70-80° C. and stirred overnight. The progress of reaction was monitored by TLC (Note 1). After completion of the reaction, water was added to the reaction mixture, and extracted with ethyl acetate (2×100 mL). The combined organic layers were concentrated in vacuo to get the crude product. The crude product was dissolved in dichloromethane and washed with water, and then brine, dried over sodium sulfate. The organic layer was concentrated in vacuo to get the crude product. The crude product was purified by column chromatography using 230-400 mesh silica gel. A solvent gradient of ethyl acetate in hexanes (10-45%) was used to elute the product from the column. All fractions containing the desired pure product were combined and concentrated in vacuo to give pure 6-propyloxy-1-hexanol (lot D-1029-048, 1.9 g, 25%) Completion of the reaction was monitored by thin layer chromatography (TLC); (eluent: 60% ethyl acetate in hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748460B2
Source datasetuspto-grants-2014_06
ORD IDord-0f268a15eb7a4982b04b66c6fed7a70b
Source noteuspto-grants-2014_06