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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956582Generated: November 1, 2026

4-tert-Butylphenol → 2-[4-(Tert-Butyl)Phenoxy]Benzenecarbaldehyde

https://huagongshe.com/reaction/1956582

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
Reactanto-FluorobenzaldehydeHCID 67970—
Product2-[4-(Tert-Butyl)Phenoxy]BenzenecarbaldehydeHCID 276342677%

Reaction Steps

Preparation analogous to Example 12 a) from 2-fluoro-benzaldehyde and 4-tert-butylphenol. Yield: 77%, yellow oil after high vacuum distillation (93°-100° C., 0.9 mbar); TLC (silica gel; hexane/ethyl acetate=1:1; UV): Rf =0.65; 1H-NMR (CDCl3, 200 MHz): 1.35 (s, 9H); 6.75-7.55 (m, 7H); 7.92 (dd, 1H); 10.50 (s, 1H); MS: 254 (M+), 239.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780500
Source datasetuspto-grants-1998_07
ORD IDord-4381b2611d6243b6b117bb9ccb0906a3
Source noteuspto-grants-1998_07