HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636364Generated: October 26, 2026
Tin tetrachloride → Stannous chloride dihydrate
https://huagongshe.com/reaction/636364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | (2,3-Dichloro-6-nitrophenyl)methanamine hydrochloride | HCID 21255093 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Stannous chloride dihydrate | HCID 61436 | — |
| Product | 2-(Aminomethyl)-3,4-dichloroaniline | HCID 5200350 | — |
Reaction Steps
A solution of 7.131 g of tin (II) chloride dihydrate in 4.7 L of concentrated hydrochloric acid was prepared. Separately, 1.631 g of 2,3-dichloro-6-nitrobenzylamine hydrochloride was dissolved in 9.5 L of concentrated hydrochloric acid. The solution of the amine was added to the tin chloride solution over 1-2 hours to maintain the reaction temperature below 45° C. The mixture was stirred for 2 hours at 40-45° C. in a warm water bath, and cooled in an ice/methanol bath to −5° C. The mixture was filtered, and the isolated solids slurried with 13 L water, 6.5 kg ice, and 6 L methylene chloride. Sodium hydroxide (50% aqueous solution) was added until pH >12, and the organic layer was removed. The aqueous phase was extracted with methylene chloride (2×6 L), and the combined organic layers washed with water (6 L portions) until pH=7-8. The organic layers were dried over magnesium sulfate (500 g) and charcoal (200 g) for 16 hours, and filtered. The filtrate was concentrated to an oil, and crystallized from isopropanol at −20° C. to give 2-amino-5,6-dichlorobenzylamine in 58 to 96% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06194420B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-71fb8237d79f47c49bcdf0a4ccb2b509 |
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| Source note | uspto-grants-2001_02 |
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