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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285030Generated: November 1, 2026

Thionyl Chloride → HCID 20186261, compound

https://huagongshe.com/reaction/1285030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20186268HCID 20186268—
CatalystPyridineHCID 1049—
SolventBenzeneHCID 241—
ProductHCID 20186261HCID 20186261—

Reaction Steps

Next, 0.82 g of Li[AlH4 ] was added to 50 ml of dried (C2H5)2O, and the resulting mixture was stirred. Thereto was gradually added 5 g of 4-[p-(2-hydroxycarbonylethyl)phenyl]pentylcyclohexane. Thereafter the thus obtained mixture was stirred for 5 hours, and filtered. The (C2H5)2O was distilled off from the filtrate, and the residue was recrystallized from n--C6H14 to obtain 4-[p-(3-hydroxypropyl)phenyl]pentylcyclohexane. The melting point of this compound was 70.7° to 72.5° C. To a mixture of 3.6 g of SOCl2, one drop of pyridine and 50 ml of benzene was added 4.3 g of the 4-[p-(3-hydroxypropyl)phenyl]pentylcyclohexane obtained above, and the resulting mixture was refluxed for 5 hours. Thereafter, the surplus SOCl2 was distilled off to obtain 4-[p-(3-chloropropyl)phenyl]pentylcyclohexane. The melting point of this compound was 70.7° to 72.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564694
Source datasetuspto-grants-1986_01
ORD IDord-4baccc49d80149f78e82b1f7a513b883
Source noteuspto-grants-1986_01