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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295351Generated: November 1, 2026

tert-Butanol → Racemic [2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hex-1-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1295351

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-Phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carboxylic acidHCID 58907323—
ProductRacemic [2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hex-1-yl]-carbamic acid tert-butyl esterHCID 6933728234%

Reaction Steps

In a round bottomed flask were combined the starting material racemic 2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carboxylic acid (0.36 g, 1.0 mmol) and tert-butyl alcohol (5 mL). Triethylamine (0.28 mL, 2.0 mmol) and diphenylphosphoryl azide (0.3 mL, 1.4 mmol) were added and the reaction was placed in an 83° C. oil bath and allowed to reflux gently under nitrogen for 16 hours. Most of the tert-butyl alcohol was removed at reduced pressure and the residue was partitioned between saturated sodium bicarbonate solution and EtOAc. The organics were washed with brine, dried over calcium sulfate, filtered and concentrated to an oil which was flash chromatographed on silica gel using 10%-20% ETOAc/Hexanes to give [2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hex-1-yl]-carbamic acid tert-butyl ester (0.14 g, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241798B2
Source datasetuspto-grants-2007_07
ORD IDord-e5231f34a1c64d239394f0d41c0253e0
Source noteuspto-grants-2007_07