HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016446Generated: October 30, 2026
Sodium borohydride → 4-Chloro-2,6-dimethylbenzyl alcohol
https://huagongshe.com/reaction/1016446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18406975 | HCID 18406975 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Chloro-2,6-dimethylbenzyl alcohol | HCID 69545701 | — |
Reaction Steps
Dissolve 4-chloro-2,6-dimethyl benzaldehyde (5.0 g, 168.64 g/mol) in 100 mL dry MeOH. Cool to 0° C. while stirring under N2. Portionwise add powdered NaBH4 (0.76 g, 37.85 g/mol) over 5 min. Stir at 0° C. for 2 h, monitoring by TLC until aldehyde consumed, then evaporate to a yellow oil. Add H2O (50 mL) and bring to pH 7.0 by addition of saturated NH4Cl. Extract the neutral aqueous layer with CH2Cl2 (3×75 mL) and dry the pooled organic layers over Na2SO4. Filter and concentrate to a yellow oil. Flush through a pad of silica to remove baseline material, then evaporate to a yellow solid (3.0 g) which can be used without further purification. LCMS=171.6 (MH+), 169.6 (M−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06476038B1 |
|---|
| Source dataset | uspto-grants-2002_11 |
|---|
| ORD ID | ord-4d8a3256ddf647b881ebd1bce13721a3 |
|---|
| Source note | uspto-grants-2002_11 |
|---|