HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355200Generated: October 29, 2026
Sodium borohydride → HCID 70434749, compound
https://huagongshe.com/reaction/355200
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20214926 | HCID 20214926 | — |
| Reactant | HCID 20214946 | HCID 20214946 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70434749 | HCID 70434749 | 50.4% |
Reaction Steps
A mixture of 9.3 gm of 2,5-dichloro-4-hydroxyphenylglyoxal hydrate, 7.25 gm of 1-(3-amino-3-methylbutyl)-benzimidazole and 100 ml of alcohol was stirred for 3 hours at 40°-45° C. The resulting solution was subsequently cooled, admixed in portions with 8 gm of sodium borohydride, and the mixture was stirred for 3 hours at room temperature. After the addition of 100 ml of methanol for decomposition of the sodium borohydride, the mixture was allowed to stand for 10 hours, the solvent was distilled off under reduced pressure, the residue was dissolved in 200 ml of water, and the solution was acidified with concentrated hydrochloric acid. 9.5 gm of 1-(2,5-dichloro-4-hydroxyphenyl)-2-[4-(1-benzimidazolyl)-2-methyl-2-butylamino]-ethanol dihydrochloride×1 H2O, m.p. 180°-183° C., of the formula ##STR33## were obtained. The yield was 50.4% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04378361 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-2edd5ff5e4e34511bc7a7bf869ab5ac1 |
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| Source note | uspto-grants-1983_03 |
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