HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487730Generated: October 30, 2026
Sodium borohydride → HCID 19093003, compound
https://huagongshe.com/reaction/487730
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,3,4-Trimethoxy-6-nitrobenzaldehyde | HCID 12320031 | — |
| Product | HCID 19093003 | HCID 19093003 | 90.9% |
Reaction Steps
Sodium borohydride (4.44 g. 0.12 mol) was added portionwise to a suspension of 2-nitro-4,5,6-trimethoxybenzaldehyde (24.2 g, 0.1 mol) in 200 ml during 0.5 hours at 5-10 ° C. in an ice-bath. The mixture was stirred for an additional 10 minutes, and the excess of NaBH4 was destroyed by addition of acetic acid. The mixture was then concentrated in vacuo to dryness, and the solid residue was triturated with water. The solid was collected by filtration, washed with water and recrystallized from ethanol to give 22.1 g (90.9%) of 2-hydroxymethyl-1-nitro-3,4,5-trimethoxybenzene; mp 69-70° C. 1H-NMR (CDCl3): δ2.89 (1H, b, exchangeable, OH) 3.94, 3.96, and 3.97 (each 3H, s, 3×OMe), 4.78 (2h, s, CH2), 7.38 (1H, s, H-6). Analyses: Calculated for C10H13NO6 : C, 49.38; H, 5.39; N, 5.76. Found: C, 49.44; H, 5.43; N, 5.79.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05296602 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-1e295e59ac1742dd8da70bcd64456338 |
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| Source note | uspto-grants-1994_03 |
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