HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398330Generated: October 29, 2026
2-Naphthalenesulfonyl chloride → HCID 23002656, compound
https://huagongshe.com/reaction/398330
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (1,2,3,4-Tetrahydroisoquinolin-1-yl)acetic acid | HCID 2733683 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23002656 | HCID 23002656 | — |
Reaction Steps
1.91 g of (1,2,3,4-tetrahydro-1-isoquinolyl)-acetic acid (Preparation 2.18) are suspended in 25 ml of dioxane, 10 ml of 1N NaOH are added, followed by portionwise addition of 2.3 g of 2-naphthalenesulphonyl chloride, and the mixture is maintained at pH=10.5-12 by addition of 1N NaOH. The mixture is kept stirring at a constant pH for 2 hours at RT. The reaction medium is diluted with 100 ml of water and is then washed twice with EtOAc and brought to pH=1.2 by addition of 6N HCl in the presence of EtOAc. This mixture is extracted with EtOAc, washed with saturated NaCl solution, dried over Na2SO4 and evaporated to dryness. The expected product crystallizes from heptane, and is drained, washed with heptane and then dried to give 3.14 g, m.p.=132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610882B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-57cfa01a8ff444f289eeeff2e5df4108 |
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| Source note | uspto-grants-2003_08 |
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