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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872309Generated: October 31, 2026

Sodium borohydride → HCID 178509566, compound

https://huagongshe.com/reaction/1872309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18329222HCID 18329222—
ReactantHCID 178509565HCID 178509565—
SolventDiethyl ether methanolHCID 21864698—
ProductHCID 178509566HCID 17850956695.2%

Reaction Steps

The polymerization of 3-[4-[4'-[(E)-2-methoxycarbonyl-vinyl]-biphenyl-4-yl]-cyclohexyl]-propyl trans-2-methyl-acrylate to poly [1-[3-[4-[4'-[(E)-2-methoxycarbonyl-vinyl]-biphenyl-4-yl]-cyclohexyl]-propoxycarbonyl]-1-methyl-ethylene] was effected analogously to Example 1. The polymer has the following phase succession (° C.): G 156 C 208 l The 3-[4-[4'-[(E)-2-methoxycarbonyl-vinyl]-biphenyl-4-yl]-cyclohexyl]-propyl trans-2-methyl-acrylate used as the starting material was prepared according to the following procedure: ##STR28## A solution of 12 g of trans-4'-[4-(3-oxo-propyl)-cyclohexyl]-biphenyl-4-carbonitrile (preparation: Mol. Cryst. Liq. Cryst. 1985, Vol. 131, 327) in 100 ml methanol/ether (9:1) was added dropwise at 0° C. within 5 minutes to a suspension of 1.39 g of sodium borohydride in 30 ml of methanol/ether (9:1). After 45 minutes a further 1 g of sodium borohydride was added. After a further hour the reaction was interrupted and the mixture was partitioned between methylene chloride and 1N hydrochloric acid. Thereupon, the organic phase was washed several times with water, dried over magnesium sulphate, filtered and evaporated. Crystallization from ethyl acetate/methylene chloride gave 11.5 g of trans-4'-[4-(3-hydroxy-propyl)-cyclohexyl]-biphenyl-4-carbonitrile as yellowish crystals. ##STR29##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107427
Source datasetuspto-grants-2000_08
ORD IDord-fc38d0d9b8d74eeab08db688017bf4fa
Source noteuspto-grants-2000_08