HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980826Generated: November 2, 2026
Dicyclohexylcarbodiimide → HCID 18597345, compound
https://huagongshe.com/reaction/1980826
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18597345 | HCID 18597345 | 81.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04511504 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-93867f289c8742f3ba4ad0a79cc26952 |
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| Source note | uspto-grants-1985_04 |
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