HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → tert-Butyl benzoyloxycarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | tert-butyl N-hydroxycarbamate | HCID 97534 | — |
| Product | tert-Butyl benzoyloxycarbamate | HCID 10037153 | — |
Reaction Steps
[(tert-Butoxy)carbonyl]amino benzoate is prepared from benzoyl chloride and N-tert-butoxycarbonyl hydroxylamine according to Scheme 1 described by Carpino et al. J. Am. Chem. Soc. 1959, 955-957. (7.2 g, 80%), 1H NMR (250 MHz, DMSO-d6) δ ppm 10.89 (1H, br. s.), 7.90-8.12 (2H, m), 7.68-7.82 (1H, m), 7.51-7.65 (2H, m), 1.43 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09018411B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-246e88cf79d44bb89dca4e21efbc04fa |
| Source note | uspto-grants-2015_04 |