HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448823Generated: October 31, 2026
Water → Benzenemethanamine, 2-chloro-N-(4-methoxyphenyl)-
https://huagongshe.com/reaction/1448823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzenemethanamine, 2-chloro-N-(4-methoxyphenyl)- | HCID 11075784 | — |
Reaction Steps
A solution of 2-chlorobenzaldehyde (70 g.) and 4-methoxyaniline (61.5 g.) in toluene (750 ml.) was refluxed under a Dean and Stark separator until no more water collected (ca. 1 hour). The toluene was evaporated in vacuo, and the residue was dissolved in methanol (1.5 l.). The methanolic solution was treated at room temperature with sodium borohydride (60 g.) added portionwise so that, with gentle cooling, the temperature was maintained at 40°-50° C. The solution was then refluxed for 15 minutes, diluted with water (1.5 l.), and the aqueous mixture extracted with ether (3×200 ml.). The combined ethereal extracts were washed with water (2×100 ml.), dried (K2CO3), and evaporated to give N-(4-methoxyphenyl)-2-chlorobenzylamine as a brown oil, Infra Red ν max 3400, 1618 cm.-1, which was used directly in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04187310 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-eecd614889cc4ae5af3b9b0141ac3607 |
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| Source note | uspto-grants-1980_02 |
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