HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(tert-Butoxycarbonyl)-L-cysteine methyl ester → Boc-Cysteinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(tert-Butoxycarbonyl)-L-cysteine methyl ester | HCID 10977409 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Cysteinol | HCID 29925397 | — |
Reaction Steps
A solution of methyl N-(tert-butoxycarbonyl)-L-cysteinate (2.6 g, 11.0 mmol) in THF (10 ml) stirred at 0° C. under N2 was treated with slow addition of a 1M solution of LiAlH4 in THF (20 mL, 20 mmol). The reaction mixture was slowly warmed up to room temperature and further stirred for 2 h, cooled to 0° C. and quenched with slow addition of water, then poured on a 15% solution of K2CO3 in water (25 mL), shaken well and extracted with DCM (3×100 mL), the organic layers were combined and dried over MgSO4, filtered and concentrated to afford the title compound as colorless oil, kept under N2 atmosphere all the times and used fresh without further purification. Assumed quantitative yield. MS: m/z=230.1 (MNa+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187415B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-45c185afecf944238ed7d5420c09a384 |
| Source note | uspto-grants-2015_11 |