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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
Reactantm-benzoyl-L-phenylalanineHCID 14233367—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductN-BOC-m-Benzoyl-L-PhenylalanineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762881
Source datasetuspto-grants-1988_08
ORD IDord-0315a666c64b43fd98a8efb3ebeb32e5
Source noteuspto-grants-1988_08