HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940293Generated: October 29, 2026
Thionyl Chloride → 3-(Cyclopentyloxy)-4-methoxybenzoyl chloride
https://huagongshe.com/reaction/1940293
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(Cyclopentyloxy)-4-methoxybenzoic acid | HCID 2779323 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(Cyclopentyloxy)-4-methoxybenzoyl chloride | HCID 2794600 | — |
Reaction Steps
Stirring thionyl chloride (20 mL) is treated portionwise with 3-cyclopentyloxy-4-methoxybenzoic acid (5.0 g; that is prepared as described hereinbefore in Reference Example 2) and the solution is then heated at 85° C. for 3 hours. Toluene (50 mL) is added and the mixture is concentrated to give 3-cyclopentyloxy-4-methoxybenzoyl chloride (4.12 g) in the form of an oil which slowly crystallized. [NMR(CDCl3): 1.6-1.7 (m,2H),1.8-1.95(m,4H),1.94-2.05(m,2H),3.94(s,3H),4.85 (m,1H),6.9(d,1H),7.55(d,1H),7.8(q,1); Elemental analysis: C,61.3; H,5.94; Cl,13.9%; Calculated: C,61.3; H,5.94; Cl,13.92%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698711 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-60a3b07cd00e4938af6f3ee2677a0301 |
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| Source note | uspto-grants-1997_12 |
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