HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857212Generated: October 31, 2026
Hydrochloric Acid → 2-(3-Bromobenzyl)-1,3-propanediol
https://huagongshe.com/reaction/857212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl (3-bromobenzyl)malonate | HCID 11056569 | — |
| Reactant | Hydride toluene | HCID 86595848 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-Bromobenzyl)-1,3-propanediol | HCID 21866948 | 48.7% |
Reaction Steps
To an ice-cooled 94 ml of 1.0 M diisobutylalminium hydride toluene solution was added dropwise 5.41 g of diethyl (3-bromobenzyl)malonate at 15° C. or less under argon flow. The mixture was stirred for 30 minutes under ice-cooling, warmed to room temperature and stirred for 2 hours. The reaction solution was ice-cooled, and 21 ml of methanol was added dropwise slowly, then 41 ml of 2 N hydrochloric acid was added dropwise. The mixture was stirred for 20 minutes at room temperature. The reaction solution was filtered to remove insolubles, extracted with ethyl acetate, washed with saturated sodium hydrogen carbonate, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (Wakogel® C-200, chloroform: methanol=10:1) to provide 1.96 g of the objective compound as white crystals. M.p. 61-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144906B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-b057ceb4ef7f4f249eed97f2dea138a0 |
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| Source note | uspto-grants-2006_12 |
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