HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4,4,4-Trinitro-1-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4,4,4-Trinitrobutyraldehyde | HCID 14401765 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4,4,4-Trinitro-1-butanol | HCID 13897974 | 63% |
Reaction Steps
Crude 4,4,4-trinitrobutaldehyde (878 g, 4.24 mol) was dissolved in methanol (1000 mL) and cooled in an ice bath while NaBH4 (130.7 g 3.44 mol) was added portion-wise. The mixture was stirred at room temperature overnight under a nitrogen purge which removed much of the solvent. The thick suspension was hydrolyzed with 6N HCl (approx. 4 L) and the product extracted with CH2Cl2 (3×100 mL). The extracts were washed with water (1000 mL), saturated NaHCO3 (2×1000 mL), and water (1000 mL). The product solution was dried (MgSO4) and concentrated to yield 554 g (63%) of a yellow oil, n=1.4735 (19° C.). The infrared spectrum showed peaks at 3619, 3370, 2950, 2890, 1595, 1305, 1058 and 801 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04795593 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-794c6a063f284aac9d7f33b3544df7e1 |
| Source note | uspto-grants-1989_01 |