HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393763Generated: October 29, 2026
Naphthalene → 3,3-Dimethyl-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/2393763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 18977225 | HCID 18977225 | — |
| Solvent | Dimethoxymethane | HCID 8020 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3,3-Dimethyl-1,2,3,4-tetrahydroisoquinoline | HCID 10986556 | 86% |
Reaction Steps
To a stirred solution of naphthalene (5.8 g, 0.045 mol) in dimethoxyethane (50 mL) was added sodium metal (1.09 g, 0.039 mol.). The mixture was allowed to stir for four (4) hours until a dark green color persisted. To this was added of N-toluenesulfonyl-3,3-dimethyl-1,2,3,4-tetrahydroisoquinoline (5.0 g, 0.016 mol.) in 20 mL of dimethoxymethane. The reaction was monitored by gas chromatography. When the reaction was complete (≈2 hours), the mixture was quenched with saturated sodium chloride (70 mL). The mixture was partitioned between ethyl acetate (250 mL) and 10% HCL (250 mL) and the organic layer was discarded. 10% Sodium hydroxide was added to the aqueous layer until a pH=7 was obtained. The aqueous layer was further extracted over methylene chloride (2×100 mL), dried over magnesium sulfate, filtered and concentrated (25° C./150 torr) to produce 2.2 g (86%) of 3,3-dimethyl-1,2,3,4-tetrahydroisoquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05808071 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-bbc5d5d97eb746e68fb48c9c8d11df52 |
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| Source note | uspto-grants-1998_09 |
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