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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292778Generated: October 31, 2026

Di-tert-butyl dicarbonate → tert-Butyl (5-methoxy-2-methylphenyl)carbamate

https://huagongshe.com/reaction/2292778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant5-Methoxy-o-toluidineHCID 99500—
ReactantTert-butyl N-[5-methoxy-2-(2-oxopropyl)phenyl]carbamateHCID 10707784—
Producttert-Butyl (5-methoxy-2-methylphenyl)carbamateHCID 1060992080%

Reaction Steps

1-[2-(tert-Butoxycarbonylamino)-4-methoxyphenyl]-2-propanone. 12 g (87 mmol) of 5-methoxy-2-methylaniline was treated by the method in Example 1, Part A, with 19 g (87 mmol)of di-tert-butyl dicarbonate to give on concentrating a reaction mixture containing 16.4 g (80% yield) of N-tert-butoxycarbonyl-5-methoxy-2-methylaniline. This material (69 mmol) was reacted with 106 mL of 1.3M sec-butyl lithium in cyclohexane and then 7.1 g (69 mmol) of N-methoxy-N-methylacetamide (as described in Example 9, Part B) to give after chromatography on silica, eluting with 33% EtOAc/hexane, 13.8 g (72% yield) of 1-[2-(tert-butoxycarbonylamino-4-methoxyphenyl]-2-propanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684034
Source datasetuspto-grants-1997_11
ORD IDord-be0415326e7942ff8aaf9de813d1d366
Source noteuspto-grants-1997_11