HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → (R)-benzyl 1-(4-chlorobutanamido)-3-hydroxypropan-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59201592 | HCID 59201592 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-benzyl 1-(4-chlorobutanamido)-3-hydroxypropan-2-ylcarbamate | HCID 86639450 | 85% |
Reaction Steps
To a solution of (R)-methyl 2-(benzyloxycarbonylamino)-3-(4-chlorobutanamido)propanoate (5.0 g, 14 mmol) in 100 mL of anhydrous MeOH was added NaBH4 (12.9 g, 0.33 mol) and the mixture was stirred at it overnight. The pH of the reaction mixture was adjusted to 8-9 using NaHCO3, the mixture was evaporated to near dryness, followed by extraction with EtOAc. The organic layer was washed with water, dried over Na2SO4, filtered and concentrated to give (R)-benzyl 1-(4-chlorobutanamido)-3-hydroxypropan-2-ylcarbamate (3.9 g, yield 85%) that was used in the next step without further purification. 1H NMR (CDCl3, 400 MHz) δ 7.37-7.30 (m, 5H) 5.13 (d, 2H), 3.77 (m, 1H), 3.57 (m, 4H), 2.32 (t, 2H), 2.08 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487108B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-ad12cc33fd41444ba8d4e1d5cdcbac6b |
| Source note | uspto-grants-2013_07 |