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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067100Generated: October 25, 2026

Benzaldehyde → HCID 101104055, compound

https://huagongshe.com/reaction/1067100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6993436—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 101104055HCID 101104055—

Reaction Steps

A solution of Nδ-Boc-ornithine (7.0 g), 2M sodium hydroxide (20 ml), benzaldehyde (3.2 ml) and methanol (10 ml) was cooled to 0° C. and sodium borohydride (2.7 g) was added. After 1 hr at 0° C., the mixture was kept at 25° C. for 12 h. Water (100 ml) was added and the mixture extracted with ether (2×60 ml). The combined organic extract was washed with sat. sodium bicarbonate (ca. 150 ml) and water, and dried over anhydrous sodium sulfate. After concentration in vacuo, the desired product (4.5 g) was obtained as a white solid: 1H NMR (400 MHz, CD3OD) δ1.42 (s, 9H), 1.60 (m, 2H), 1.84 (m, 2H), 3.03 (m, 2H), 3.50 (t, J=7.4 Hz, 1H), 4.11 (d, J=11.9 Hz, 1H), 4.21 (d, J=11.9 Hz, 1H), 7.41 (m, 3H), and 7.49 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245746B1
Source datasetuspto-grants-2001_06
ORD IDord-4a3a99e99369426c9f31187f82c89fa7
Source noteuspto-grants-2001_06