HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856945Generated: October 29, 2026
Sulfuryl chloride → HCID 21864949, compound
https://huagongshe.com/reaction/856945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 21864957 | HCID 21864957 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21864949 | HCID 21864949 | — |
Reaction Steps
In a 100 mL round-bottom flask was placed 5,6,7,8-tetrahydro-3-cyano-2-naphthol (1.0 g, 5.77 mmol, 1 eq, from Method II-2) in 20 mL of dry acetonitrile under argon. Sulfuryl chloride (6.09 mL, 28.85 mmol, 5.0 eq) was added dropwise. The reaction was stirred at rt for 18 h. The reaction mixture was concentrated and purified on silica gel (flash column chromatography) eluting with 20% ethyl acetate-hexane. A 1:1 diastereomeric mixture of 4-Chloro-3-hydroxy-5,6,7,8-tetrahydro-naphthalene-2-carbonitrile and 1-Chloro-3-hydroxy-5,6,7,8-tetrahydro-naphthalene-2-carbonitrile was obtained as a yellow liquid (887 mg, 66.6%, isomer ratio: 1:1). 1H-NMR (CD3CN) δ 7.81 (s, 1H), 3.24 (m, 1H), 2.66 (m, 1H), 2.33 (m, 1H), 2.07(m, 2H), 1.88 (m, 2H), 1.43 (m, 1H). GC-MS (M+=207).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144885B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-951ab5d223ca4a0dacc57024ef1650d0 |
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| Source note | uspto-grants-2006_12 |
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