HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fmoc-Gly-OH → 3-Phenylprop-2-en-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fmoc-Gly-OH | HCID 93124 | — |
| Reactant | Benzene, (3-chloro-1-propenyl)- | HCID 94242 | — |
| Product | 3-Phenylprop-2-en-1-amine | HCID 20369 | — |
Reaction Steps
Aminomethyl styrene resin was prepared from chloromethyl styrene resin (Polumer Laboratories, PL-CMS Resin, 1.0 meq/g) using the procedure of Weinshenker. Weinshenker, N. M.; Shen, C. M.; Wong, J. Y., Organic Synthesis, vol. 56, pp. 95-99. The aminomethyl resin was coupled with N-(Fmoc)glycine using a procedure similar to that described in Example 7. The Fmoc group was removed using a procedure similar to that described in Example 8. This sequence was repeated three times to give the title compound, which has three glycine residues attached to the polystyrene resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05786218 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-a6342c0f17364bb08e19dd57cb7b2e2c |
| Source note | uspto-grants-1998_07 |