HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34686Generated: October 26, 2026
Triethylamine → N-BOC-m-Benzoyl-L-Phenylalanine
https://huagongshe.com/reaction/34686
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | m-benzoyl-L-phenylalanine | HCID 14233367 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-BOC-m-Benzoyl-L-Phenylalanine | HCID 14233370 | — |
Reaction Steps
A suspension of 2.175 g of m-benzoyl-L-phenylalanine in 25 ml of water and 1.15 g of triethylamine was treated with 3.35 g of BOC-ON in 40 ml of acetone. After 3 h, acetone was removed and the aqueous residue was extracted three times with ether (discarded). The aqueous solution was acidified to pH 2 with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried (MgSO4) and stripped. The residue was triturated for 7 days with petroleum ether. The waxy insoluble solid was triturated for 14 days with an additional portion of petroleum ether and finally for 7 days with a third portion. The resulting white solid weighed 1.786 g after vacuum drying, [α]D25 +22.2±0.9°, C=0.86 g/100 ml ethanol. Anal.: Calcd. for C21H23NO5 :C, 68.28; H, 6.28; N, 3.79. Found: C, 68.01; H, 6.49; N, 3.68.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762881 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-0315a666c64b43fd98a8efb3ebeb32e5 |
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| Source note | uspto-grants-1988_08 |
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