Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414070Generated: October 31, 2026

Methanesulfonyl chloride → HCID 57038968, compound

https://huagongshe.com/reaction/414070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 14304678HCID 14304678—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 57038968HCID 5703896879.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred , ice-cooled suspension of (S)-6,7,8,9-tetrahydro-2-(3-hydroxypropyl)-2H-naphtho[2,3-b][1,4] oxazin-3(4H)-one (1.15 g) in a mixture of dichloromethane (40 ml) and triethylamine (0.45 g), was added dropwise methanesulfonyl chloride (1.01 g). The whole was stirred at 0° C. for 1.5 hour, washed with water and dried over magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography on silica gel (60 g) with ethyl acetate-hexane (3:2, v/v). The resulting crystals were recrystallized from methanol to yield (S)-6,7,8,9-tetrahydro-2-(3-mesyloxypropyl)-2H-naphto[2,3-b][1,4]oxazin-3(4H)-one as colorless needles (1.19 g, 79.7%), m.p. 153°-154° C. [α]D26 +4.8° (c=0.8, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04789675
Source datasetuspto-grants-1988_12
ORD IDord-0d392cfddccd4b15918c89b999d8046f
Source noteuspto-grants-1988_12