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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882792Generated: October 31, 2026

Toluene → tert-butyl (1R,3S,4S)-3-(hydroxymethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylate

https://huagongshe.com/reaction/882792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium HydroxideHCID 14798—
Reactant(1R, 3S, 4S)-2-Boc-2-aza-bicyclo[2.2.1]heptane-3-carboxylic acid methyl esterHCID 66866671—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (1R,3S,4S)-3-(hydroxymethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylateHCID 66866104—

Reaction Steps

At −78° C. a solution of DIBAL in toluene (1.7M, 137 mmol) is added dropwise to a solution of (1R,3S,4S)-2-aza-bicyclo[2.2.1]heptane-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl ester (61.0 mmol) in THF (180 mL). After 80 min the solution is allowed to reach rt, stirred for additional 2 h and poured into a mixture of aq. NaOH solution (1.0M, 200 mL) and ice. EtOAc (150 mL) is added, the layers are separated and the aq. layer is extracted three times with EtOAc (150 mL each). The combined organic layers are washed with aq. NaOH solution (1.0M) and brine, dried over Na2SO4 and concentrated in vacuo to give a crude product which is used without further purification. LC-MS (basic): tR=0.78 min; [M+H]+=228.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236801B2
Source datasetuspto-grants-2012_08
ORD IDord-b2ce05038b2d4ac8b03cfccf3bfcfb4d
Source noteuspto-grants-2012_08