HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → (3R)-ethyl 2-(tert-butoxycarbonylamino)-3,5-dimethylnon-8-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | (3R)-ethyl 2-amino-3-ethyl-5-methylnon-8-enoate hydrochloride | HCID 86683258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3R)-ethyl 2-(tert-butoxycarbonylamino)-3,5-dimethylnon-8-enoate | HCID 86683235 | 62.5% |
Reaction Steps
A solution of (3R)-ethyl 2-amino-3-ethyl-5-methylnon-8-enoate hydrochloride (2.99 g, 10.77 mmole) in DCM (20 mL) was added DIPEA (1.08 mL, 10.77 mmole) followed by (BOC)2O (2.39 mL, 10.77 mmole) at room temperature. The reaction mass was stirred at room temperature for overnight. The reaction mass was diluted with DCM and washed with water. The organic layer was dried over anhydrous Na2SO4 and evaporated under reduced pressure to get crude compound. The crude compound was purified by column chromotography (Silica gel, 20% ethyl acetate in pet-ether) to get 2.3 g, (62.5%) of (3R)-ethyl 2-(tert-butoxycarbonylamino)-3,5-dimethylnon-8-enoate as an oily liquid. MS: MS m/z 342.4 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957203B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-d9771bda81c743d494ff75a4061f774e |
| Source note | uspto-grants-2015_02 |