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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389449Generated: October 25, 2026

1,3-Cyclohexanediol → 3-(Tert-butyldimethylsilyl)oxy-1-cyclohexanol

https://huagongshe.com/reaction/389449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexanediolHCID 10433—
Reactant2-[3-(tert-butyldimethylsilanyloxy)-cyclopentyl]-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazoleHCID 66759519—
Product3-(Tert-butyldimethylsilyl)oxy-1-cyclohexanolHCID 55707735%

Reaction Steps

The title compound was prepared in 35% yield from 1,3-cyclohexanediol by a procedure analogous to Intermediate 28, Step A. 1H NMR (300 MHz, CDCl3): δ 4.0-4.2 (m, 1H), 3.8-3.95 (m, 1H), 1.3-2.4 (m, 9H), 0.86 (s, 9H), 0.05 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-952be78ea2404a4b9f2eea420bff95c3
Source noteuspto-grants-2013_02