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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166009Generated: November 1, 2026

1,2-Dichloroethane → HCID 53955138, compound

https://huagongshe.com/reaction/1166009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHCID 22996848HCID 22996848—
ReactantHCID 54092897HCID 54092897—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 53955138HCID 53955138—

Reaction Steps

The preparation is analogous to Example 1 from 2.64 g (10 mmol) of 4-hydroxybenzoic acid 4-acryloyloxybutyl ester, 3.99 g (10 mmol) of 4′-(6-acryloyloxyhexyloxy)-3′-methoxybiphenyl-4-carboxylic acid, 0.12 g (1 mmol) of DMAP and 2.11 g (11 mmol) of EDC. Purification of the residue by chromatography on silica gel using cyclohexane/ethyl acetate (7:3) and recrystallisation once from ethanol yields 4′-(6-acryloyloxyhexyloxy)-3′-methoxybiphenyl-4-carboxylic acid 4-(4-acryloyloxybutoxycarbonyl)-phenyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613245B1
Source datasetuspto-grants-2003_09
ORD IDord-9ba2957f139848839a871eda7fd496db
Source noteuspto-grants-2003_09