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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980826Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 18597345, compound

https://huagongshe.com/reaction/1980826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBoc-L-ValineHCID 83693—
SolventDichloromethaneHCID 6344—
ProductHCID 18597345HCID 1859734581.2%

Reaction Steps

Tertiarybutyloxycarbonyl-L-valine (25 g) in dichloromethane (200 ml) was treated with 1-hydroxybenzotriazole (15.5 g) hexylamine (11.6 g) and DCC (26 g) at room temperature for 2 days. The solution was filtered and the organic phase washed with aqueous sodium hydrogen carbonate, aqueous citric acid (1M) and water, dried over sodium sulphate and concentrated in vacuo to afford tertiary butyloxy-carbonyl-L-valine N-hexylamide (28 g) which crystallised from methanol-water as needles; m.p. 74°-76° C.; (Found: C,63.8; H,10.6; N,9.4. C16H32N2O3 requires C,64.0; H,10.7; N,9.32%); νmax (Nujol): 3280 and 1630 cm-1 ; δ(CDCl3) 0.8-1 (9H,m, 3xCH3); 1.3 (8H,m,(CH2)4); 1.45 (9H,s, (CH3)3C); 2.1 (1H, m,CH(CH3)2); 3.3 (2H,m, NHCH 2); 3.9 (1H,dd, J=8 Hz and 5 Hz., α--CH); 5.2 (1H,d, J=8 Hz, CONH) and 6.26 (1H,m,NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04511504
Source datasetuspto-grants-1985_04
ORD IDord-93867f289c8742f3ba4ad0a79cc26952
Source noteuspto-grants-1985_04