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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865379Generated: November 3, 2026

Acetic Acid → HCID 54113518, compound

https://huagongshe.com/reaction/865379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 18655318HCID 18655318—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 54113518HCID 5411351896,911.797%

Reaction Steps

Nα -Boc-4-Nitrophenyl-D-alanine (209 grams, 0.68 mole) was dissolved in 500 mL of ethyl alcohol and acidified with acetic acid (10 mL). To this was added 0.65 g of 10% Pd/carbon, and the mixture was hydrogenated at about room temperature using H2 at about 40 psi until the uptake of hydrogen had ceased (6 hours). The catalyst was removed by filtration, and the reaction products were concentrated under vacuum to yield a viscous oil that solidified upon trituration with petroleum ether. The amino acid was collected by filtration, washed with petroleum ether and dried to give 184 g of Nα -Boc-4-aminophenyl-D-alanine (0,659 mole, 97%) having [α]D =-40.2° (c=1.0 in EtOAc) and -23.4° (c=1.0 in MeOH); mp=128°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565574
Source datasetuspto-grants-1996_10
ORD IDord-05c11a90788943849e68f6fa7608f838
Source noteuspto-grants-1996_10