HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Dodecanoyltetradecanoic acid → N-[(R)-3-dodecanoyloxytetradecanoyl]-L-serine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Dodecanoyltetradecanoic acid | HCID 124680 | — |
| Reactant | (S)-Benzyl 2-amino-3-hydroxypropanoate | HCID 854069 | — |
| Reactant | Edc-methiodide | HCID 86585083 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(R)-3-dodecanoyloxytetradecanoyl]-L-serine benzyl ester | HCID 53732699 | 90% |
Reaction Steps
In the same manner as described in Example 2-(5), L-serine benzyl ester (390 mg, 2.0 mmol) was acylated with (R)-3-dodecanoyloxytetradecanoic acid (935 mg, 2.2 mmol) in the presence of EDC·MeI (745 mg, 2.5 mmol) in CH2Cl2 to afford 1.08 g (90%) of N-[(R)-3-dodecanoyloxytetradecanoyl]-L-serine benzyl ester: mp 53-54° C. 1H NMR (CDCl3) δ 0.88 (t, 6H, J=6.5 Hz), 1.1-1.6 (m, 46H), 2.30 (t, 2H, J=7.7 Hz), 2.50 (d, 2H, 5.6 Hz), 2.62 (t, 1H, J=6.2 Hz), 3.97 (m, 2H), 4.65 (m, 1H), 5.19 (m, 3H), 6.63 (d, 1H, J=6.8 Hz), 7.35 (br s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07541020B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-0761d5c86e8746ea84a62a2795046ec8 |
| Source note | uspto-grants-2009_06 |