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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606545Generated: October 25, 2026

Formaldehyde → [4-[1-(Tert-butyldimethylsilanyloxy)hexyl]phenyl]methanol

https://huagongshe.com/reaction/606545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant((1-(4-Bromophenyl)hexyl)oxy)(tert-butyl)dimethylsilaneHCID 57438973—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product[4-[1-(Tert-butyldimethylsilanyloxy)hexyl]phenyl]methanolHCID 6704610469%

Reaction Steps

tert-Butyllithium (6.6 mL of a 1.7 M solution in pentane, 11.32 mmol) was added to a solution of the aryl bromide 7 (2.0 g, 5.39 mmol) in THF (22 mL) at −78° C. After 0.5 h paraformaldehyde (323 mg, 8.09 mmol) was added. The reaction was warmed to room temperature and stirred for 16 h. The reaction was quenched with saturated aqueous NH4Cl and extracted with EtOAc. The organic portion was dried (MgSO4), filtered and concentrated in vacuo. FCC (silica gel, 6:1 hex/EtOAc) yielded 1.2 g (69%) of the alcohol 8 as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915316B2
Source datasetuspto-grants-2011_03
ORD IDord-67fbe19536ed4065ad1c29c3c4d64a78
Source noteuspto-grants-2011_03