HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891224Generated: October 31, 2026
HCID 22244954, compound → HCID 22244957, compound
https://huagongshe.com/reaction/891224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22244954 | HCID 22244954 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22244957 | HCID 22244957 | — |
Reaction Steps
To a solution of 150 g (0.78 mol) of 3-tert-butoxy-2-methyl-2-nitro-propan-1-ol [prepared according to Example 1c or 1c′] in 700 ml of toluene in a pressure vessel is added 15 g of Raney-Ni and 40 ml of a pH 7.00 buffer [NORMEX (RTM), Carlo Erba]. Through the closed autoclave is added at room temperature hydrogen under 50-60 bar pressure. The reaction mixture is heated to 40° C. and maintained at this temperature for 8 hours. The reaction mixture is then cooled to room temperature, diluted with toluene, filtered and the filtrate concentrated using a vacuum rotary evaporator. The residue yields 2-amino-3-tert-butoxy-2-methyl-propan-1-ol (compound 301, Table 1), pale green solid, m.p. 30-35° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07002010B2 |
|---|
| Source dataset | uspto-grants-2006_02 |
|---|
| ORD ID | ord-dfb8ef1c5f7a457b9f7dca395a9ce354 |
|---|
| Source note | uspto-grants-2006_02 |
|---|