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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393410Generated: October 27, 2026

N-Boc-p-toluenesulfonamide → tert-Butyl methyl(tosyl)carbamate

https://huagongshe.com/reaction/393410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Boc-p-toluenesulfonamideHCID 688170—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventMethanolHCID 887—
Producttert-Butyl methyl(tosyl)carbamateHCID 2266006785%

Reaction Steps

The crude fluorous DEAD reagent 22 was then used in Mitsunobu reactions with N-Boc-p-toluenesulfonamide. Once again, the standard mode of addition gave complete conversion with MeOH and the product, N-methyl-N-boc-p-toluenesulfonamide was isolated in 85% yield after FSPE. However, the allyl alcohol gave only trace conversion of the starting material. The organic fraction after FSPE was mostly starting material. These results are summarized in Table 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806357B1
Source datasetuspto-grants-2004_10
ORD IDord-41a99d97be5e482e8c5bb07a1cfdf604
Source noteuspto-grants-2004_10