Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255265Generated: October 31, 2026

Methanol → (3-(4-(tert-Butyldimethylsilyloxy)but-1-ynyl)phenyl)methanol

https://huagongshe.com/reaction/1255265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(But-3-yn-1-yloxy)(tert-butyl)dimethylsilaneHCID 4304567—
Reactant3-(3-(Hydroxymethyl)phenyl)propan-1-olHCID 55267680—
SolventAmmoniaHCID 222—
Product(3-(4-(tert-Butyldimethylsilyloxy)but-1-ynyl)phenyl)methanolHCID 58168614—

Reaction Steps

Prepared by the method of Aromatic Intermediate 18, step a using tert-butyldimethyl(but-3-ynyloxy)silane (0.92 g) in place of tert-butyldimethyl(prop-2-ynyloxy)silane. The preparative HPLC conditions were changed to XBridge™, Gradient: 75-99% methanol in 0.2% aqueous ammonia to avoid cleavage of the silyl protecting group. Yield 0.79 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455483B2
Source datasetuspto-grants-2013_06
ORD IDord-9d5dc419da804c37b93b1265af03f15b
Source noteuspto-grants-2013_06