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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369821Generated: October 26, 2026

Methyl 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzoate → 3-Tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcohol

https://huagongshe.com/reaction/369821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzoateHCID 18352492—
ReactantDiisobutylaluminumhydride tolueneHCID 86583787—
SolventTolueneHCID 1140—
Product3-Tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcoholHCID 5395416490%

Reaction Steps

According to example 184, 5.00 g of methyl 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzoate was reduced using 31.8 mL of 1M diisobutylaluminum hydride/toluene and 50 mL of anhydrous toluene. Analysis of the reaction mixture by tlc after 30 min indicated some remaining starting material. To ensure complete reduction, an additional 5 mL of 1M diisobutylaluminum hydride/toluene was added and the reaction was allowed to proceed for an additional 5 min. Work-up in the usual manner afforded 4.11 g (90%) of 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcohol as a cloudy oil. The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140100
Source datasetuspto-grants-2000_10
ORD IDord-c3b729b626ff4c30aff16de73400e83d
Source noteuspto-grants-2000_10