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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350866Generated: October 31, 2026

Triphenylphosphine → Tert-butyl 4-tert-butyl-3-(cyclopropylmethoxy)phenyl carbonate

https://huagongshe.com/reaction/1350866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantCyclopropanemethanolHCID 75644—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-tert-butyl-3-hydroxyphenyl carbonateHCID 15482845—
ProductTert-butyl 4-tert-butyl-3-(cyclopropylmethoxy)phenyl carbonateHCID 2109753879.1%

Reaction Steps

Tert-butyl 4-tert-butyl-3-hydroxyphenyl carbonate (1.5 g, 5.6 mmol), cyclopropylmethanol (0.5 mL, 6.2 mmol), triphenylphosphine (1.6 g, 6.2 mmol) and diethyl azodicarboxylate (DEAD) (1.0 mL, 6.2 mmol) were treated in the same procedure described in Example 31(a). The crude residue was applied to a silica gel chromatography column and eluted with a volume mixture of hexane and ethyl acetate (19/1 to 9/1) to furnish 1.42 g (79% yield) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214824B2
Source datasetuspto-grants-2007_05
ORD IDord-de5c770a597c41a290d781575f944ef7
Source noteuspto-grants-2007_05