HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289248Generated: October 30, 2026
Chlorosulfonic acid → HCID 135622211, compound
https://huagongshe.com/reaction/2289248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | HCID 135838122 | HCID 135838122 | — |
| Product | HCID 135622211 | HCID 135622211 | 41% |
Reaction Steps
1,2,5,6-tetrahydro-3-methyl-1-oxobenzo[f]quinazoline (5 g, 0.024 mole) was added to chlorosulfonic acid (50 ml, Aldrich) and stirred for 12 hours at room temperature. The reaction mixture was poured over ice (750 g), and the dark brown solid collected by filtration. The solid was washed with water, suspended in water (500 ml), and the pH of the suspension adjusted to 5.00 by addition of sodium bicarbonate. The suspension was filtered, the product washed with H2 0 and dried under high vacuum at room temperature to give 1,2,5,6-tetrahydro-3-methyl- oxobenzo[f]quinazolin-9-sulfonyl chloride as a light brown solid (3.054 g, 41%). 1H NMR (DMSO-d6, 300 MHz) δ: 2.60 (s, 3H, CH3); 2.90 (s, 4H, Ar CH2); 7.22 (d, J=9Hz, 1H, Ar); 7.53 (d, J=9Hz, 1H, Ar); 8.75 (s, 1H, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090941 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-b1b357b2471c4227aaae85f9d6781df2 |
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| Source note | uspto-grants-2000_07 |
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