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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66628Generated: October 26, 2026

1-Phenylethanol → 4-(1-Phenylethyl)-2,6-ditert-butyl-phenol

https://huagongshe.com/reaction/66628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylethanolHCID 7409—
Reactant2,6-Di-tert-butylphenolHCID 31405—
SolventAcetic AcidHCID 176—
SolventFormic AcidHCID 284—
Product4-(1-Phenylethyl)-2,6-ditert-butyl-phenolHCID 331193—

Reaction Steps

2,6-Di-t-butyl-4-(α-methylbenzyl) phenol was prepared by refluxing 2,6-di-t-butylphenol (51 g) and 1-phenylethanol (31 g) in acetic acid (40 ml) and formic acid (75 ml) as described for A. The product was obtained as a colorless oil, b.p. 166°-168° at 1.0 mm Hg (62 g); (meas. mass=310.2309. Calc. for C22H30O=310.2296). The pmr spectrum was: δ1.40, 18H, S; δ1.61, 3H, D (J=8 Hz); δ4.06, 1H, Q (J=8 Hz); δ5.02, 1H, S; δ7.01, 2H, S; δ7.22, 5H, S.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342777
Source datasetuspto-grants-1982_08
ORD IDord-6a959fd9b2ad4e44acf5d89ceaea591e
Source noteuspto-grants-1982_08