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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954534Generated: November 1, 2026

HCID 23433467, compound → HCID 22279055, compound

https://huagongshe.com/reaction/1954534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23433467HCID 23433467—
ReactantHCID 23433515HCID 23433515—
ProductHCID 22279055HCID 2227905599%

Reaction Steps

This compound was prepared from 6-tert-butyloxycarbamoyl-2-nitrotoluene (4.60 g, 18.2 mmol) in a manner similar to that described for 3-tert-butyloxycarbamoylaniline (EXAMPLE 147), affording 4.00 g (99%) of 2-amino-6-tert-butyloxycarbamoyltoluene as a colorless oil. Data for 2-amino-6-tert-butyloxycarbamoyltoluene: 1H NMR (400 MHz, CDCl3) 7.04 (br d of ABq, JAB =8.0, JA =0, JB =7.9, 2 H, 5,4-H), 6.49 (d, J=8.3, 1 H, 3-H), 6.26 (br s, 1 H, NH), 3.61 (br s, 2 H, NH2), 2.02 (s, 3 H, 1-CH3), 1.51 [s, 9 H, (CH3)3CO)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121450
Source datasetuspto-grants-2000_09
ORD IDord-03965df0e3a44b3a8478f676ceac5252
Source noteuspto-grants-2000_09