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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231801Generated: October 31, 2026

Hydrochloric Acid → HCID 13878907, compound

https://huagongshe.com/reaction/2231801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13878906HCID 13878906—
SolventWaterHCID 962—
ProductHCID 13878907HCID 1387890799.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 30 g of 4'-octyloxy-4-formylbiphenyl, 2.0 g of sodium borohydride and 300 ml of isopropanol was stirred on a water bath maintained at 70° C. for 3 hours. 20 ml of 6 N hydrochloric acid and 10 ml of water were added, and the resulting mixture was stirred for 2 hours. The reaction mixture was allowed to cool and filtered to collect solids. These solids were recrystallized from 300 ml of ethanol to obtain 30 g of 4'-octyloxy-4-hydroxymethyl-biphenyl. The total of 4'-octyloxy-4-hydroxymethyl-biphenyl, 100 ml of toluene and 40 g of thionyl chloride were uniformly mixed and allowed to stand overnight at room temperature. Then, the mixture was heated for 30 minutes on a water bath maintained at 70° C. After being allowed to cool, the mixture was poured into ice water and then extracted with 300 ml of toluene. The extract was washed with saturated saline water, with a saturated aqueous sodium hydrogen-carbonate and further with saturated saline water to make it neutral. Then, the extract was dried over anhydrous magnesium sulfate, concentrated and then recrystallized from 300 ml of ethanol to obtain 26 g of 4'-octyloxy-4-chloromethyl-biphenyl having a melting point of 97.3 to 98.0° C. Analysis of the compound by HPLC showed that the purity was 99.6%. (ii) Preparation of Objective Compound

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04784791
Source datasetuspto-grants-1988_11
ORD IDord-e7858eb46ed64fe5818b0cf6c3ad3e4a
Source noteuspto-grants-1988_11