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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-Phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carboxylic acid | HCID 58907323 | — |
| Product | Racemic [2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hex-1-yl]-carbamic acid tert-butyl ester | HCID 69337282 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241798B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-e5231f34a1c64d239394f0d41c0253e0 |
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| Source note | uspto-grants-2007_07 |
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